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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: 2-85395194-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=85395194&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 85395194,
      "ref": "T",
      "alt": "C",
      "effect": "intron_variant",
      "transcript": "NM_001747.4",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "CAPG",
          "gene_hgnc_id": 1474,
          "hgvs_c": "c.982-236A>G",
          "hgvs_p": null,
          "transcript": "NM_001747.4",
          "protein_id": "NP_001738.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 348,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1047,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1250,
          "mane_select": "ENST00000263867.9",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001747.4"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "CAPG",
          "gene_hgnc_id": 1474,
          "hgvs_c": "c.982-236A>G",
          "hgvs_p": null,
          "transcript": "ENST00000263867.9",
          "protein_id": "ENSP00000263867.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 348,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1047,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1250,
          "mane_select": "NM_001747.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000263867.9"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "CAPG",
          "gene_hgnc_id": 1474,
          "hgvs_c": "c.982-236A>G",
          "hgvs_p": null,
          "transcript": "ENST00000409724.5",
          "protein_id": "ENSP00000386965.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 348,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1047,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1151,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000409724.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "CAPG",
          "gene_hgnc_id": 1474,
          "hgvs_c": "c.937-236A>G",
          "hgvs_p": null,
          "transcript": "ENST00000409921.5",
          "protein_id": "ENSP00000387063.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 333,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1002,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1195,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000409921.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "CAPG",
          "gene_hgnc_id": 1474,
          "hgvs_c": "c.982-92A>G",
          "hgvs_p": null,
          "transcript": "ENST00000951335.1",
          "protein_id": "ENSP00000621394.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 396,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1191,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1382,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000951335.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "CAPG",
          "gene_hgnc_id": 1474,
          "hgvs_c": "c.982-92A>G",
          "hgvs_p": null,
          "transcript": "ENST00000951337.1",
          "protein_id": "ENSP00000621396.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 396,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1191,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1390,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000951337.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "CAPG",
          "gene_hgnc_id": 1474,
          "hgvs_c": "c.982-212A>G",
          "hgvs_p": null,
          "transcript": "ENST00000880826.1",
          "protein_id": "ENSP00000550885.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 356,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1071,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1303,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000880826.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "CAPG",
          "gene_hgnc_id": 1474,
          "hgvs_c": "c.982-212A>G",
          "hgvs_p": null,
          "transcript": "ENST00000880833.1",
          "protein_id": "ENSP00000550892.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 356,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1071,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1243,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000880833.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 10,
          "intron_rank": 9,
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          "gene_symbol": "CAPG",
          "gene_hgnc_id": 1474,
          "hgvs_c": "c.982-212A>G",
          "hgvs_p": null,
          "transcript": "ENST00000880841.1",
          "protein_id": "ENSP00000550900.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 356,
          "cds_start": null,
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          "cds_length": 1071,
          "cdna_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000880841.1"
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        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 10,
          "intron_rank": 9,
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          "gene_symbol": "CAPG",
          "gene_hgnc_id": 1474,
          "hgvs_c": "c.982-236A>G",
          "hgvs_p": null,
          "transcript": "NM_001256139.2",
          "protein_id": "NP_001243068.1",
          "transcript_support_level": null,
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          "aa_length": 348,
          "cds_start": null,
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        {
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          "gene_symbol": "CAPG",
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          "hgvs_c": "c.982-236A>G",
          "hgvs_p": null,
          "transcript": "NM_001320732.2",
          "protein_id": "NP_001307661.1",
          "transcript_support_level": null,
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          "cds_start": null,
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          "cdna_start": null,
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          "canonical": false,
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        {
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          "gene_symbol": "CAPG",
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          "gene_symbol": "CAPG",
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          "transcript": "ENST00000880842.1",
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        {
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For research and educational, non-commercial use only. Not for clinical or diagnostic use. GeneBe does not provide medical advice. Data use for AI modeling is prohibited: if used, the cost is $0.001 per byte of downloaded uncompressed data.