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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: 11-70486021-G-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=70486021&ref=G&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 70486021,
      "ref": "G",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "ENST00000601538.6",
      "consequences": [
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SHANK2",
          "gene_hgnc_id": 14295,
          "hgvs_c": "c.4272C>A",
          "hgvs_p": "p.Pro1424Pro",
          "transcript": "NM_012309.5",
          "protein_id": "NP_036441.2",
          "transcript_support_level": null,
          "aa_start": 1424,
          "aa_end": null,
          "aa_length": 1849,
          "cds_start": 4272,
          "cds_end": null,
          "cds_length": 5550,
          "cdna_start": 4537,
          "cdna_end": null,
          "cdna_length": 10830,
          "mane_select": "ENST00000601538.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SHANK2",
          "gene_hgnc_id": 14295,
          "hgvs_c": "c.4272C>A",
          "hgvs_p": "p.Pro1424Pro",
          "transcript": "ENST00000601538.6",
          "protein_id": "ENSP00000469689.2",
          "transcript_support_level": 5,
          "aa_start": 1424,
          "aa_end": null,
          "aa_length": 1849,
          "cds_start": 4272,
          "cds_end": null,
          "cds_length": 5550,
          "cdna_start": 4537,
          "cdna_end": null,
          "cdna_length": 10830,
          "mane_select": "NM_012309.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SHANK2",
          "gene_hgnc_id": 14295,
          "hgvs_c": "c.2484C>A",
          "hgvs_p": "p.Pro828Pro",
          "transcript": "ENST00000409161.5",
          "protein_id": "ENSP00000386491.1",
          "transcript_support_level": 1,
          "aa_start": 828,
          "aa_end": null,
          "aa_length": 1253,
          "cds_start": 2484,
          "cds_end": null,
          "cds_length": 3762,
          "cdna_start": 2917,
          "cdna_end": null,
          "cdna_length": 9208,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 23,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SHANK2",
          "gene_hgnc_id": 14295,
          "hgvs_c": "c.4392C>A",
          "hgvs_p": "p.Pro1464Pro",
          "transcript": "NM_001441024.1",
          "protein_id": "NP_001427953.1",
          "transcript_support_level": null,
          "aa_start": 1464,
          "aa_end": null,
          "aa_length": 1889,
          "cds_start": 4392,
          "cds_end": null,
          "cds_length": 5670,
          "cdna_start": 4657,
          "cdna_end": null,
          "cdna_length": 10950,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SHANK2",
          "gene_hgnc_id": 14295,
          "hgvs_c": "c.4221C>A",
          "hgvs_p": "p.Pro1407Pro",
          "transcript": "NM_001441025.1",
          "protein_id": "NP_001427954.1",
          "transcript_support_level": null,
          "aa_start": 1407,
          "aa_end": null,
          "aa_length": 1832,
          "cds_start": 4221,
          "cds_end": null,
          "cds_length": 5499,
          "cdna_start": 4486,
          "cdna_end": null,
          "cdna_length": 10779,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 23,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SHANK2",
          "gene_hgnc_id": 14295,
          "hgvs_c": "c.4221C>A",
          "hgvs_p": "p.Pro1407Pro",
          "transcript": "NM_001441026.1",
          "protein_id": "NP_001427955.1",
          "transcript_support_level": null,
          "aa_start": 1407,
          "aa_end": null,
          "aa_length": 1832,
          "cds_start": 4221,
          "cds_end": null,
          "cds_length": 5499,
          "cdna_start": 4613,
          "cdna_end": null,
          "cdna_length": 10906,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SHANK2",
          "gene_hgnc_id": 14295,
          "hgvs_c": "c.4221C>A",
          "hgvs_p": "p.Pro1407Pro",
          "transcript": "NM_001441027.1",
          "protein_id": "NP_001427956.1",
          "transcript_support_level": null,
          "aa_start": 1407,
          "aa_end": null,
          "aa_length": 1832,
          "cds_start": 4221,
          "cds_end": null,
          "cds_length": 5499,
          "cdna_start": 4746,
          "cdna_end": null,
          "cdna_length": 11039,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SHANK2",
          "gene_hgnc_id": 14295,
          "hgvs_c": "c.4221C>A",
          "hgvs_p": "p.Pro1407Pro",
          "transcript": "NM_001441028.1",
          "protein_id": "NP_001427957.1",
          "transcript_support_level": null,
          "aa_start": 1407,
          "aa_end": null,
          "aa_length": 1832,
          "cds_start": 4221,
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          "cds_length": 5499,
          "cdna_start": 4610,
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          "cdna_length": 10903,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
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        },
        {
          "aa_ref": "P",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 23,
          "exon_rank_end": null,
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          "intron_rank": null,
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          "gene_symbol": "SHANK2",
          "gene_hgnc_id": 14295,
          "hgvs_c": "c.4221C>A",
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          "transcript": "NM_001441029.1",
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          "transcript_support_level": null,
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          "cdna_start": 4619,
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          "mane_select": null,
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        {
          "aa_ref": "P",
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          "protein_coding": true,
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          "consequences": [
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          ],
          "exon_rank": 22,
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          "exon_count": 23,
          "intron_rank": null,
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          "gene_symbol": "SHANK2",
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          "hgvs_c": "c.4221C>A",
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        {
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        {
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          "gene_symbol": "SHANK2",
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          "hgvs_c": "c.3135C>A",
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        {
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