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GeneBe API Showcase

This page demonstrates how to use the GeneBe API to query variant information. The API provides programmatic access to genomic annotations and variant data.

API presented here should be used for checking single variants. If you want to check many variants at once, please use other API endpoints that you will find in the documentation.

Documentation & Advanced Usage

Complete API documentation:docs.genebe.net/docs/api/overview/

Interactive endpoint tester:api.genebe.net/cloud/gb-api-doc/swagger-ui/

Python client for pandas:pypi.org/project/genebe/

Java CLI for VCF files:github.com/pstawinski/genebe-cli

All tools documented at:docs.genebe.net

API Request Examples for Variant: 7-87452976-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=87452976&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "7",
      "pos": 87452976,
      "ref": "G",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "ENST00000649586.2",
      "consequences": [
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCB4",
          "gene_hgnc_id": 45,
          "hgvs_c": "c.504C>T",
          "hgvs_p": "p.Asn168Asn",
          "transcript": "NM_000443.4",
          "protein_id": "NP_000434.1",
          "transcript_support_level": null,
          "aa_start": 168,
          "aa_end": null,
          "aa_length": 1279,
          "cds_start": 504,
          "cds_end": null,
          "cds_length": 3840,
          "cdna_start": 557,
          "cdna_end": null,
          "cdna_length": 4293,
          "mane_select": "ENST00000649586.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCB4",
          "gene_hgnc_id": 45,
          "hgvs_c": "c.504C>T",
          "hgvs_p": "p.Asn168Asn",
          "transcript": "ENST00000649586.2",
          "protein_id": "ENSP00000496956.2",
          "transcript_support_level": null,
          "aa_start": 168,
          "aa_end": null,
          "aa_length": 1279,
          "cds_start": 504,
          "cds_end": null,
          "cds_length": 3840,
          "cdna_start": 557,
          "cdna_end": null,
          "cdna_length": 4293,
          "mane_select": "NM_000443.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCB4",
          "gene_hgnc_id": 45,
          "hgvs_c": "c.504C>T",
          "hgvs_p": "p.Asn168Asn",
          "transcript": "ENST00000265723.8",
          "protein_id": "ENSP00000265723.4",
          "transcript_support_level": 1,
          "aa_start": 168,
          "aa_end": null,
          "aa_length": 1286,
          "cds_start": 504,
          "cds_end": null,
          "cds_length": 3861,
          "cdna_start": 616,
          "cdna_end": null,
          "cdna_length": 4020,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCB4",
          "gene_hgnc_id": 45,
          "hgvs_c": "c.504C>T",
          "hgvs_p": "p.Asn168Asn",
          "transcript": "ENST00000359206.8",
          "protein_id": "ENSP00000352135.3",
          "transcript_support_level": 1,
          "aa_start": 168,
          "aa_end": null,
          "aa_length": 1279,
          "cds_start": 504,
          "cds_end": null,
          "cds_length": 3840,
          "cdna_start": 588,
          "cdna_end": null,
          "cdna_length": 3961,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCB4",
          "gene_hgnc_id": 45,
          "hgvs_c": "n.511C>T",
          "hgvs_p": null,
          "transcript": "ENST00000473795.1",
          "protein_id": null,
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1115,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCB4",
          "gene_hgnc_id": 45,
          "hgvs_c": "c.504C>T",
          "hgvs_p": "p.Asn168Asn",
          "transcript": "NM_018849.3",
          "protein_id": "NP_061337.1",
          "transcript_support_level": null,
          "aa_start": 168,
          "aa_end": null,
          "aa_length": 1286,
          "cds_start": 504,
          "cds_end": null,
          "cds_length": 3861,
          "cdna_start": 557,
          "cdna_end": null,
          "cdna_length": 4314,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCB4",
          "gene_hgnc_id": 45,
          "hgvs_c": "c.504C>T",
          "hgvs_p": "p.Asn168Asn",
          "transcript": "NM_018850.3",
          "protein_id": "NP_061338.1",
          "transcript_support_level": null,
          "aa_start": 168,
          "aa_end": null,
          "aa_length": 1232,
          "cds_start": 504,
          "cds_end": null,
          "cds_length": 3699,
          "cdna_start": 557,
          "cdna_end": null,
          "cdna_length": 4152,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCB4",
          "gene_hgnc_id": 45,
          "hgvs_c": "c.504C>T",
          "hgvs_p": "p.Asn168Asn",
          "transcript": "ENST00000453593.5",
          "protein_id": "ENSP00000392983.1",
          "transcript_support_level": 5,
          "aa_start": 168,
          "aa_end": null,
          "aa_length": 1232,
          "cds_start": 504,
          "cds_end": null,
          "cds_length": 3699,
          "cdna_start": 504,
          "cdna_end": null,
          "cdna_length": 3699,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCB4",
          "gene_hgnc_id": 45,
          "hgvs_c": "c.504C>T",
          "hgvs_p": "p.Asn168Asn",
          "transcript": "XM_011516308.4",
          "protein_id": "XP_011514610.4",
          "transcript_support_level": null,
          "aa_start": 168,
          "aa_end": null,
          "aa_length": 1294,
          "cds_start": 504,
          "cds_end": null,
          "cds_length": 3885,
          "cdna_start": 767,
          "cdna_end": null,
          "cdna_length": 4374,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCB4",
          "gene_hgnc_id": 45,
          "hgvs_c": "c.504C>T",
          "hgvs_p": "p.Asn168Asn",
          "transcript": "XM_011516309.4",
          "protein_id": "XP_011514611.4",
          "transcript_support_level": null,
          "aa_start": 168,
          "aa_end": null,
          "aa_length": 1287,
          "cds_start": 504,
          "cds_end": null,
          "cds_length": 3864,
          "cdna_start": 767,
          "cdna_end": null,
          "cdna_length": 4353,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCB4",
          "gene_hgnc_id": 45,
          "hgvs_c": "c.504C>T",
          "hgvs_p": "p.Asn168Asn",
          "transcript": "XM_047420475.1",
          "protein_id": "XP_047276431.1",
          "transcript_support_level": null,
          "aa_start": 168,
          "aa_end": null,
          "aa_length": 1247,
          "cds_start": 504,
          "cds_end": null,
          "cds_length": 3744,
          "cdna_start": 557,
          "cdna_end": null,
          "cdna_length": 4023,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCB4",
          "gene_hgnc_id": 45,
          "hgvs_c": "c.504C>T",
          "hgvs_p": "p.Asn168Asn",
          "transcript": "XM_047420476.1",
          "protein_id": "XP_047276432.1",
          "transcript_support_level": null,
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          "aa_end": null,
          "aa_length": 1197,
          "cds_start": 504,
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          "cdna_start": 557,
          "cdna_end": null,
          "cdna_length": 4047,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCB4",
          "gene_hgnc_id": 45,
          "hgvs_c": "c.504C>T",
          "hgvs_p": "p.Asn168Asn",
          "transcript": "XM_047420477.1",
          "protein_id": "XP_047276433.1",
          "transcript_support_level": null,
          "aa_start": 168,
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          "cds_start": 504,
          "cds_end": null,
          "cds_length": 2754,
          "cdna_start": 767,
          "cdna_end": null,
          "cdna_length": 3103,
          "mane_select": null,
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          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCB4",
          "gene_hgnc_id": 45,
          "hgvs_c": "n.447C>T",
          "hgvs_p": null,
          "transcript": "ENST00000643670.1",
          "protein_id": "ENSP00000496629.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 2284,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
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          "gene_symbol": "ABCB4",
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          "hgvs_c": "n.504C>T",
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          "transcript": "ENST00000644106.1",
          "protein_id": "ENSP00000493477.1",
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          "mane_select": null,
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        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCB4",
          "gene_hgnc_id": 45,
          "hgvs_c": "n.767C>T",
          "hgvs_p": null,
          "transcript": "XR_001744810.3",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 2892,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCB4",
          "gene_hgnc_id": 45,
          "hgvs_c": "n.767C>T",
          "hgvs_p": null,
          "transcript": "XR_007060045.1",
          "protein_id": null,
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          "cdna_length": 8596,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
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          "gene_symbol": "ABCB4",
          "gene_hgnc_id": 45,
          "hgvs_c": "n.767C>T",
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          "transcript": "XR_007060046.1",
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          "mane_select": null,
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        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCB4",
          "gene_hgnc_id": 45,
          "hgvs_c": "n.767C>T",
          "hgvs_p": null,
          "transcript": "XR_007060047.1",
          "protein_id": null,
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          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
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          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCB4",
          "gene_hgnc_id": 45,
          "hgvs_c": "n.767C>T",
          "hgvs_p": null,
          "transcript": "XR_007060048.1",
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          "aa_start": null,
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          "cdna_start": null,
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          "cdna_length": 8609,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ABCB4",
          "gene_hgnc_id": 45,
          "hgvs_c": "n.767C>T",
          "hgvs_p": null,
          "transcript": "XR_007060049.1",
          "protein_id": null,
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      ],
      "gene_symbol": "ABCB4",
      "gene_hgnc_id": 45,
      "dbsnp": "rs1202283",
      "frequency_reference_population": 0.51978916,
      "hom_count_reference_population": 228424,
      "allele_count_reference_population": 838449,
      "gnomad_exomes_af": 0.53041,
      "gnomad_genomes_af": 0.41764,
      "gnomad_exomes_ac": 775002,
      "gnomad_genomes_ac": 63447,
      "gnomad_exomes_homalt": 211967,
      "gnomad_genomes_homalt": 16457,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.7400000095367432,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.009999999776482582,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.74,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.744,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.01,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -21,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BA1",
      "acmg_by_gene": [
        {
          "score": -21,
          "benign_score": 21,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BP7",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000649586.2",
          "gene_symbol": "ABCB4",
          "hgnc_id": 45,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "SD,AR,AD",
          "hgvs_c": "c.504C>T",
          "hgvs_p": "p.Asn168Asn"
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      ],
      "clinvar_disease": " 3, intrahepatic, of pregnancy,Cholestasis,Progressive familial intrahepatic cholestasis type 3,not provided,not specified",
      "clinvar_classification": "Benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "B:9",
      "phenotype_combined": "not specified|Cholestasis, intrahepatic, of pregnancy, 3|Progressive familial intrahepatic cholestasis type 3|not provided",
      "pathogenicity_classification_combined": "Benign",
      "custom_annotations": null
    }
  ],
  "message": null
}