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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: 6-129514556-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=129514556&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "6",
      "pos": 129514556,
      "ref": "G",
      "alt": "A",
      "effect": "missense_variant",
      "transcript": "ENST00000421865.3",
      "consequences": [
        {
          "aa_ref": "A",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 64,
          "exon_rank_end": null,
          "exon_count": 65,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LAMA2",
          "gene_hgnc_id": 6482,
          "hgvs_c": "c.9172G>A",
          "hgvs_p": "p.Ala3058Thr",
          "transcript": "NM_000426.4",
          "protein_id": "NP_000417.3",
          "transcript_support_level": null,
          "aa_start": 3058,
          "aa_end": null,
          "aa_length": 3122,
          "cds_start": 9172,
          "cds_end": null,
          "cds_length": 9369,
          "cdna_start": 9280,
          "cdna_end": null,
          "cdna_length": 9696,
          "mane_select": "ENST00000421865.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "T",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 64,
          "exon_rank_end": null,
          "exon_count": 65,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LAMA2",
          "gene_hgnc_id": 6482,
          "hgvs_c": "c.9172G>A",
          "hgvs_p": "p.Ala3058Thr",
          "transcript": "ENST00000421865.3",
          "protein_id": "ENSP00000400365.2",
          "transcript_support_level": 5,
          "aa_start": 3058,
          "aa_end": null,
          "aa_length": 3122,
          "cds_start": 9172,
          "cds_end": null,
          "cds_length": 9369,
          "cdna_start": 9280,
          "cdna_end": null,
          "cdna_length": 9696,
          "mane_select": "NM_000426.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 65,
          "exon_rank_end": null,
          "exon_count": 66,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LAMA2",
          "gene_hgnc_id": 6482,
          "hgvs_c": "c.9436G>A",
          "hgvs_p": "p.Ala3146Thr",
          "transcript": "ENST00000618192.5",
          "protein_id": "ENSP00000480802.2",
          "transcript_support_level": 5,
          "aa_start": 3146,
          "aa_end": null,
          "aa_length": 3210,
          "cds_start": 9436,
          "cds_end": null,
          "cds_length": 9633,
          "cdna_start": 9544,
          "cdna_end": null,
          "cdna_length": 9960,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 63,
          "exon_rank_end": null,
          "exon_count": 64,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LAMA2",
          "gene_hgnc_id": 6482,
          "hgvs_c": "c.9160G>A",
          "hgvs_p": "p.Ala3054Thr",
          "transcript": "NM_001079823.2",
          "protein_id": "NP_001073291.2",
          "transcript_support_level": null,
          "aa_start": 3054,
          "aa_end": null,
          "aa_length": 3118,
          "cds_start": 9160,
          "cds_end": null,
          "cds_length": 9357,
          "cdna_start": 9268,
          "cdna_end": null,
          "cdna_length": 9684,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 63,
          "exon_rank_end": null,
          "exon_count": 64,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LAMA2",
          "gene_hgnc_id": 6482,
          "hgvs_c": "c.9160G>A",
          "hgvs_p": "p.Ala3054Thr",
          "transcript": "ENST00000617695.5",
          "protein_id": "ENSP00000481744.2",
          "transcript_support_level": 5,
          "aa_start": 3054,
          "aa_end": null,
          "aa_length": 3118,
          "cds_start": 9160,
          "cds_end": null,
          "cds_length": 9357,
          "cdna_start": 9268,
          "cdna_end": null,
          "cdna_length": 9656,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LAMA2",
          "gene_hgnc_id": 6482,
          "hgvs_c": "c.1237G>A",
          "hgvs_p": "p.Ala413Thr",
          "transcript": "ENST00000494137.2",
          "protein_id": "ENSP00000510626.1",
          "transcript_support_level": 3,
          "aa_start": 413,
          "aa_end": null,
          "aa_length": 477,
          "cds_start": 1237,
          "cds_end": null,
          "cds_length": 1434,
          "cdna_start": 1637,
          "cdna_end": null,
          "cdna_length": 2015,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LAMA2",
          "gene_hgnc_id": 6482,
          "hgvs_c": "c.1237G>A",
          "hgvs_p": "p.Ala413Thr",
          "transcript": "ENST00000498257.6",
          "protein_id": "ENSP00000510533.1",
          "transcript_support_level": 5,
          "aa_start": 413,
          "aa_end": null,
          "aa_length": 477,
          "cds_start": 1237,
          "cds_end": null,
          "cds_length": 1434,
          "cdna_start": 1485,
          "cdna_end": null,
          "cdna_length": 1901,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LAMA2",
          "gene_hgnc_id": 6482,
          "hgvs_c": "c.1237G>A",
          "hgvs_p": "p.Ala413Thr",
          "transcript": "ENST00000688799.1",
          "protein_id": "ENSP00000508458.1",
          "transcript_support_level": null,
          "aa_start": 413,
          "aa_end": null,
          "aa_length": 477,
          "cds_start": 1237,
          "cds_end": null,
          "cds_length": 1434,
          "cdna_start": 1334,
          "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": 9,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LAMA2",
          "gene_hgnc_id": 6482,
          "hgvs_c": "n.2150G>A",
          "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": 7,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LAMA2",
          "gene_hgnc_id": 6482,
          "hgvs_c": "n.4045G>A",
          "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": 7,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LAMA2",
          "gene_hgnc_id": 6482,
          "hgvs_c": "n.1509G>A",
          "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.806+7921C>T",
          "hgvs_p": null,
          "transcript": "ENST00000657779.1",
          "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": 3385,
          "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": 11,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000226149",
          "gene_hgnc_id": null,
          "hgvs_c": "n.1110+7921C>T",
          "hgvs_p": null,
          "transcript": "ENST00000659721.1",
          "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": 1444,
          "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": 12,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000226149",
          "gene_hgnc_id": null,
          "hgvs_c": "n.1099+7921C>T",
          "hgvs_p": null,
          "transcript": "ENST00000664071.1",
          "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": 1445,
          "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.788+7921C>T",
          "hgvs_p": null,
          "transcript": "ENST00000665046.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 2743,
          "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": 11,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000226149",
          "gene_hgnc_id": null,
          "hgvs_c": "n.1105+7921C>T",
          "hgvs_p": null,
          "transcript": "ENST00000668058.1",
          "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": 1578,
          "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": 8,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000226149",
          "gene_hgnc_id": null,
          "hgvs_c": "n.751-3722C>T",
          "hgvs_p": null,
          "transcript": "ENST00000670413.1",
          "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": 1362,
          "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": 5,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000226149",
          "gene_hgnc_id": null,
          "hgvs_c": "n.471-11765C>T",
          "hgvs_p": null,
          "transcript": "ENST00000810118.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 726,
          "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": 9,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000226149",
          "gene_hgnc_id": null,
          "hgvs_c": "n.796-3722C>T",
          "hgvs_p": null,
          "transcript": "ENST00000810119.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 1455,
          "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": 5,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000226149",
          "gene_hgnc_id": null,
          "hgvs_c": "n.573-11765C>T",
          "hgvs_p": null,
          "transcript": "ENST00000810120.1",
          "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": 830,
          "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": 7,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "LOC102723409",
          "gene_hgnc_id": null,
          "hgvs_c": "n.14823+7921C>T",
          "hgvs_p": null,
          "transcript": "XR_001743859.2",
          "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,
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      "clinvar_disease": "LAMA2-related muscular dystrophy",
      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "US:1",
      "phenotype_combined": "LAMA2-related muscular dystrophy",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
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  "message": null
}