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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: 6-129505238-T-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=129505238&ref=T&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "6",
      "pos": 129505238,
      "ref": "T",
      "alt": "G",
      "effect": "stop_gained",
      "transcript": "ENST00000421865.3",
      "consequences": [
        {
          "aa_ref": "Y",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 61,
          "exon_rank_end": null,
          "exon_count": 65,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LAMA2",
          "gene_hgnc_id": 6482,
          "hgvs_c": "c.8586T>G",
          "hgvs_p": "p.Tyr2862*",
          "transcript": "NM_000426.4",
          "protein_id": "NP_000417.3",
          "transcript_support_level": null,
          "aa_start": 2862,
          "aa_end": null,
          "aa_length": 3122,
          "cds_start": 8586,
          "cds_end": null,
          "cds_length": 9369,
          "cdna_start": 8694,
          "cdna_end": null,
          "cdna_length": 9696,
          "mane_select": "ENST00000421865.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "*",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 61,
          "exon_rank_end": null,
          "exon_count": 65,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LAMA2",
          "gene_hgnc_id": 6482,
          "hgvs_c": "c.8586T>G",
          "hgvs_p": "p.Tyr2862*",
          "transcript": "ENST00000421865.3",
          "protein_id": "ENSP00000400365.2",
          "transcript_support_level": 5,
          "aa_start": 2862,
          "aa_end": null,
          "aa_length": 3122,
          "cds_start": 8586,
          "cds_end": null,
          "cds_length": 9369,
          "cdna_start": 8694,
          "cdna_end": null,
          "cdna_length": 9696,
          "mane_select": "NM_000426.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 62,
          "exon_rank_end": null,
          "exon_count": 66,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LAMA2",
          "gene_hgnc_id": 6482,
          "hgvs_c": "c.8850T>G",
          "hgvs_p": "p.Tyr2950*",
          "transcript": "ENST00000618192.5",
          "protein_id": "ENSP00000480802.2",
          "transcript_support_level": 5,
          "aa_start": 2950,
          "aa_end": null,
          "aa_length": 3210,
          "cds_start": 8850,
          "cds_end": null,
          "cds_length": 9633,
          "cdna_start": 8958,
          "cdna_end": null,
          "cdna_length": 9960,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 60,
          "exon_rank_end": null,
          "exon_count": 64,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LAMA2",
          "gene_hgnc_id": 6482,
          "hgvs_c": "c.8574T>G",
          "hgvs_p": "p.Tyr2858*",
          "transcript": "NM_001079823.2",
          "protein_id": "NP_001073291.2",
          "transcript_support_level": null,
          "aa_start": 2858,
          "aa_end": null,
          "aa_length": 3118,
          "cds_start": 8574,
          "cds_end": null,
          "cds_length": 9357,
          "cdna_start": 8682,
          "cdna_end": null,
          "cdna_length": 9684,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 60,
          "exon_rank_end": null,
          "exon_count": 64,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LAMA2",
          "gene_hgnc_id": 6482,
          "hgvs_c": "c.8574T>G",
          "hgvs_p": "p.Tyr2858*",
          "transcript": "ENST00000617695.5",
          "protein_id": "ENSP00000481744.2",
          "transcript_support_level": 5,
          "aa_start": 2858,
          "aa_end": null,
          "aa_length": 3118,
          "cds_start": 8574,
          "cds_end": null,
          "cds_length": 9357,
          "cdna_start": 8682,
          "cdna_end": null,
          "cdna_length": 9656,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LAMA2",
          "gene_hgnc_id": 6482,
          "hgvs_c": "c.651T>G",
          "hgvs_p": "p.Tyr217*",
          "transcript": "ENST00000494137.2",
          "protein_id": "ENSP00000510626.1",
          "transcript_support_level": 3,
          "aa_start": 217,
          "aa_end": null,
          "aa_length": 477,
          "cds_start": 651,
          "cds_end": null,
          "cds_length": 1434,
          "cdna_start": 1051,
          "cdna_end": null,
          "cdna_length": 2015,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LAMA2",
          "gene_hgnc_id": 6482,
          "hgvs_c": "c.651T>G",
          "hgvs_p": "p.Tyr217*",
          "transcript": "ENST00000498257.6",
          "protein_id": "ENSP00000510533.1",
          "transcript_support_level": 5,
          "aa_start": 217,
          "aa_end": null,
          "aa_length": 477,
          "cds_start": 651,
          "cds_end": null,
          "cds_length": 1434,
          "cdna_start": 899,
          "cdna_end": null,
          "cdna_length": 1901,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LAMA2",
          "gene_hgnc_id": 6482,
          "hgvs_c": "c.651T>G",
          "hgvs_p": "p.Tyr217*",
          "transcript": "ENST00000688799.1",
          "protein_id": "ENSP00000508458.1",
          "transcript_support_level": null,
          "aa_start": 217,
          "aa_end": null,
          "aa_length": 477,
          "cds_start": 651,
          "cds_end": null,
          "cds_length": 1434,
          "cdna_start": 748,
          "cdna_end": null,
          "cdna_length": 1750,
          "mane_select": null,
          "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": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LAMA2",
          "gene_hgnc_id": 6482,
          "hgvs_c": "n.1564T>G",
          "hgvs_p": null,
          "transcript": "ENST00000688198.1",
          "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": 2528,
          "mane_select": null,
          "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": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LAMA2",
          "gene_hgnc_id": 6482,
          "hgvs_c": "n.1580T>G",
          "hgvs_p": null,
          "transcript": "ENST00000690858.1",
          "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": 4443,
          "mane_select": null,
          "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": 4,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LAMA2",
          "gene_hgnc_id": 6482,
          "hgvs_c": "n.923T>G",
          "hgvs_p": null,
          "transcript": "ENST00000693461.1",
          "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": 1888,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000226149",
          "gene_hgnc_id": null,
          "hgvs_c": "n.807-2447A>C",
          "hgvs_p": null,
          "transcript": "ENST00000657779.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 3385,
          "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": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000226149",
          "gene_hgnc_id": null,
          "hgvs_c": "n.1111-2447A>C",
          "hgvs_p": null,
          "transcript": "ENST00000659721.1",
          "protein_id": null,
          "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": 1444,
          "mane_select": null,
          "mane_plus": null,
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          "feature": null
        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000226149",
          "gene_hgnc_id": null,
          "hgvs_c": "n.1100-2447A>C",
          "hgvs_p": null,
          "transcript": "ENST00000664071.1",
          "protein_id": null,
          "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": 1445,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
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          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000226149",
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          "hgvs_c": "n.789-2447A>C",
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          "transcript": "ENST00000665046.1",
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          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          ],
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          "exon_count": 11,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000226149",
          "gene_hgnc_id": null,
          "hgvs_c": "n.1106-2447A>C",
          "hgvs_p": null,
          "transcript": "ENST00000668058.1",
          "protein_id": null,
          "transcript_support_level": null,
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          "cds_start": -4,
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          "cdna_length": 1578,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000226149",
          "gene_hgnc_id": null,
          "hgvs_c": "n.471-2447A>C",
          "hgvs_p": null,
          "transcript": "ENST00000810118.1",
          "protein_id": null,
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          "cdna_length": 726,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000226149",
          "gene_hgnc_id": null,
          "hgvs_c": "n.573-2447A>C",
          "hgvs_p": null,
          "transcript": "ENST00000810120.1",
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        },
        {
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 7,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "LOC102723409",
          "gene_hgnc_id": null,
          "hgvs_c": "n.14824-2447A>C",
          "hgvs_p": null,
          "transcript": "XR_001743859.2",
          "protein_id": null,
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        },
        {
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          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 8,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "LOC102723409",
          "gene_hgnc_id": null,
          "hgvs_c": "n.12103-2447A>C",
          "hgvs_p": null,
          "transcript": "XR_001743860.2",
          "protein_id": null,
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          "aa_start": null,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 14100,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "LOC102723409",
          "gene_hgnc_id": null,
          "hgvs_c": "n.12103-2447A>C",
          "hgvs_p": null,
          "transcript": "XR_007059754.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_start": -4,
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      "clinvar_classification": "Pathogenic",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "P:1",
      "phenotype_combined": "LAMA2-related muscular dystrophy",
      "pathogenicity_classification_combined": "Pathogenic",
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  "message": null
}