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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: 10-102363085-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=102363085&ref=A&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "10",
      "pos": 102363085,
      "ref": "A",
      "alt": "G",
      "effect": "intron_variant",
      "transcript": "ENST00000369983.5",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": 15,
          "intron_rank_end": null,
          "gene_symbol": "GBF1",
          "gene_hgnc_id": 4181,
          "hgvs_c": "c.1877-171A>G",
          "hgvs_p": null,
          "transcript": "NM_001377137.1",
          "protein_id": "NP_001364066.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1860,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5583,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6403,
          "mane_select": "ENST00000369983.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": 15,
          "intron_rank_end": null,
          "gene_symbol": "GBF1",
          "gene_hgnc_id": 4181,
          "hgvs_c": "c.1877-171A>G",
          "hgvs_p": null,
          "transcript": "ENST00000369983.5",
          "protein_id": "ENSP00000359000.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1860,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5583,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6403,
          "mane_select": "NM_001377137.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 38,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "GBF1",
          "gene_hgnc_id": 4181,
          "hgvs_c": "n.3105A>G",
          "hgvs_p": null,
          "transcript": "ENST00000679280.1",
          "protein_id": null,
          "transcript_support_level": null,
          "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": 7436,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": 16,
          "intron_rank_end": null,
          "gene_symbol": "GBF1",
          "gene_hgnc_id": 4181,
          "hgvs_c": "c.1973-171A>G",
          "hgvs_p": null,
          "transcript": "NM_001411027.1",
          "protein_id": "NP_001397956.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1892,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5679,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6499,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": 16,
          "intron_rank_end": null,
          "gene_symbol": "GBF1",
          "gene_hgnc_id": 4181,
          "hgvs_c": "c.1973-171A>G",
          "hgvs_p": null,
          "transcript": "ENST00000673650.1",
          "protein_id": "ENSP00000501233.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1892,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5679,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6502,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": 16,
          "intron_rank_end": null,
          "gene_symbol": "GBF1",
          "gene_hgnc_id": 4181,
          "hgvs_c": "c.1973-171A>G",
          "hgvs_p": null,
          "transcript": "NM_001391922.1",
          "protein_id": "NP_001378851.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1888,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5667,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6487,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": 16,
          "intron_rank_end": null,
          "gene_symbol": "GBF1",
          "gene_hgnc_id": 4181,
          "hgvs_c": "c.1949-171A>G",
          "hgvs_p": null,
          "transcript": "NM_001411003.1",
          "protein_id": "NP_001397932.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1884,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5655,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6475,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": 16,
          "intron_rank_end": null,
          "gene_symbol": "GBF1",
          "gene_hgnc_id": 4181,
          "hgvs_c": "c.1949-171A>G",
          "hgvs_p": null,
          "transcript": "ENST00000674034.1",
          "protein_id": "ENSP00000501064.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1884,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5655,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6478,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": 15,
          "intron_rank_end": null,
          "gene_symbol": "GBF1",
          "gene_hgnc_id": 4181,
          "hgvs_c": "c.1874-171A>G",
          "hgvs_p": null,
          "transcript": "NM_001377141.1",
          "protein_id": "NP_001364070.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 1859,
          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
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          "feature": null
        },
        {
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          "strand": true,
          "consequences": [
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          "exon_count": 40,
          "intron_rank": 15,
          "intron_rank_end": null,
          "gene_symbol": "GBF1",
          "gene_hgnc_id": 4181,
          "hgvs_c": "c.1874-171A>G",
          "hgvs_p": null,
          "transcript": "NM_004193.3",
          "protein_id": "NP_004184.1",
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          "aa_start": null,
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        {
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          "gene_symbol": "GBF1",
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          "canonical": false,
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          "gene_symbol": "GBF1",
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          "gene_symbol": "GBF1",
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      "clinvar_classification": "",
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}