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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: 3-11036957-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=11036957&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "3",
      "pos": 11036957,
      "ref": "C",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "ENST00000287766.10",
      "consequences": [
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC6A1",
          "gene_hgnc_id": 11042,
          "hgvs_c": "c.1791C>T",
          "hgvs_p": "p.Ala597Ala",
          "transcript": "NM_003042.4",
          "protein_id": "NP_003033.3",
          "transcript_support_level": null,
          "aa_start": 597,
          "aa_end": null,
          "aa_length": 599,
          "cds_start": 1791,
          "cds_end": null,
          "cds_length": 1800,
          "cdna_start": 2188,
          "cdna_end": null,
          "cdna_length": 4478,
          "mane_select": "ENST00000287766.10",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC6A1",
          "gene_hgnc_id": 11042,
          "hgvs_c": "c.1791C>T",
          "hgvs_p": "p.Ala597Ala",
          "transcript": "ENST00000287766.10",
          "protein_id": "ENSP00000287766.4",
          "transcript_support_level": 1,
          "aa_start": 597,
          "aa_end": null,
          "aa_length": 599,
          "cds_start": 1791,
          "cds_end": null,
          "cds_length": 1800,
          "cdna_start": 2188,
          "cdna_end": null,
          "cdna_length": 4478,
          "mane_select": "NM_003042.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC6A1",
          "gene_hgnc_id": 11042,
          "hgvs_c": "c.1863C>T",
          "hgvs_p": "p.Ala621Ala",
          "transcript": "ENST00000698198.1",
          "protein_id": "ENSP00000513602.1",
          "transcript_support_level": null,
          "aa_start": 621,
          "aa_end": null,
          "aa_length": 623,
          "cds_start": 1863,
          "cds_end": null,
          "cds_length": 1872,
          "cdna_start": 1944,
          "cdna_end": null,
          "cdna_length": 4161,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC6A1",
          "gene_hgnc_id": 11042,
          "hgvs_c": "c.1818C>T",
          "hgvs_p": "p.Ala606Ala",
          "transcript": "ENST00000644803.1",
          "protein_id": "ENSP00000494469.1",
          "transcript_support_level": null,
          "aa_start": 606,
          "aa_end": null,
          "aa_length": 608,
          "cds_start": 1818,
          "cds_end": null,
          "cds_length": 1827,
          "cdna_start": 1949,
          "cdna_end": null,
          "cdna_length": 4093,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC6A1",
          "gene_hgnc_id": 11042,
          "hgvs_c": "c.1791C>T",
          "hgvs_p": "p.Ala597Ala",
          "transcript": "NM_001348250.2",
          "protein_id": "NP_001335179.1",
          "transcript_support_level": null,
          "aa_start": 597,
          "aa_end": null,
          "aa_length": 599,
          "cds_start": 1791,
          "cds_end": null,
          "cds_length": 1800,
          "cdna_start": 2127,
          "cdna_end": null,
          "cdna_length": 4417,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC6A1",
          "gene_hgnc_id": 11042,
          "hgvs_c": "c.1791C>T",
          "hgvs_p": "p.Ala597Ala",
          "transcript": "ENST00000642201.1",
          "protein_id": "ENSP00000494778.1",
          "transcript_support_level": null,
          "aa_start": 597,
          "aa_end": null,
          "aa_length": 599,
          "cds_start": 1791,
          "cds_end": null,
          "cds_length": 1800,
          "cdna_start": 1945,
          "cdna_end": null,
          "cdna_length": 4174,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC6A1",
          "gene_hgnc_id": 11042,
          "hgvs_c": "c.1791C>T",
          "hgvs_p": "p.Ala597Ala",
          "transcript": "ENST00000642515.1",
          "protein_id": "ENSP00000496348.1",
          "transcript_support_level": null,
          "aa_start": 597,
          "aa_end": null,
          "aa_length": 599,
          "cds_start": 1791,
          "cds_end": null,
          "cds_length": 1800,
          "cdna_start": 3195,
          "cdna_end": null,
          "cdna_length": 4720,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC6A1",
          "gene_hgnc_id": 11042,
          "hgvs_c": "c.1791C>T",
          "hgvs_p": "p.Ala597Ala",
          "transcript": "ENST00000642639.1",
          "protein_id": "ENSP00000494191.1",
          "transcript_support_level": null,
          "aa_start": 597,
          "aa_end": null,
          "aa_length": 599,
          "cds_start": 1791,
          "cds_end": null,
          "cds_length": 1800,
          "cdna_start": 2162,
          "cdna_end": null,
          "cdna_length": 3934,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC6A1",
          "gene_hgnc_id": 11042,
          "hgvs_c": "c.1791C>T",
          "hgvs_p": "p.Ala597Ala",
          "transcript": "ENST00000642735.1",
          "protein_id": "ENSP00000494050.1",
          "transcript_support_level": null,
          "aa_start": 597,
          "aa_end": null,
          "aa_length": 599,
          "cds_start": 1791,
          "cds_end": null,
          "cds_length": 1800,
          "cdna_start": 2301,
          "cdna_end": null,
          "cdna_length": 4577,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC6A1",
          "gene_hgnc_id": 11042,
          "hgvs_c": "c.1791C>T",
          "hgvs_p": "p.Ala597Ala",
          "transcript": "ENST00000642767.1",
          "protein_id": "ENSP00000494346.1",
          "transcript_support_level": null,
          "aa_start": 597,
          "aa_end": null,
          "aa_length": 599,
          "cds_start": 1791,
          "cds_end": null,
          "cds_length": 1800,
          "cdna_start": 2147,
          "cdna_end": null,
          "cdna_length": 4437,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC6A1",
          "gene_hgnc_id": 11042,
          "hgvs_c": "c.1791C>T",
          "hgvs_p": "p.Ala597Ala",
          "transcript": "ENST00000642820.1",
          "protein_id": "ENSP00000495900.1",
          "transcript_support_level": null,
          "aa_start": 597,
          "aa_end": null,
          "aa_length": 599,
          "cds_start": 1791,
          "cds_end": null,
          "cds_length": 1800,
          "cdna_start": 2372,
          "cdna_end": null,
          "cdna_length": 4629,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC6A1",
          "gene_hgnc_id": 11042,
          "hgvs_c": "c.1791C>T",
          "hgvs_p": "p.Ala597Ala",
          "transcript": "ENST00000643396.1",
          "protein_id": "ENSP00000494136.1",
          "transcript_support_level": null,
          "aa_start": 597,
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          "aa_length": 599,
          "cds_start": 1791,
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          "cds_length": 1800,
          "cdna_start": 4532,
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          "cdna_length": 6767,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
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          "gene_symbol": "SLC6A1",
          "gene_hgnc_id": 11042,
          "hgvs_c": "c.1791C>T",
          "hgvs_p": "p.Ala597Ala",
          "transcript": "ENST00000643498.1",
          "protein_id": "ENSP00000494997.1",
          "transcript_support_level": null,
          "aa_start": 597,
          "aa_end": null,
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          "cds_start": 1791,
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          "cdna_start": 2240,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC6A1",
          "gene_hgnc_id": 11042,
          "hgvs_c": "c.1791C>T",
          "hgvs_p": "p.Ala597Ala",
          "transcript": "ENST00000645029.1",
          "protein_id": "ENSP00000496171.1",
          "transcript_support_level": null,
          "aa_start": 597,
          "aa_end": null,
          "aa_length": 599,
          "cds_start": 1791,
          "cds_end": null,
          "cds_length": 1800,
          "cdna_start": 2231,
          "cdna_end": null,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 17,
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          "intron_rank": null,
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          "gene_symbol": "SLC6A1",
          "gene_hgnc_id": 11042,
          "hgvs_c": "c.1791C>T",
          "hgvs_p": "p.Ala597Ala",
          "transcript": "ENST00000645054.1",
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          "cds_start": 1791,
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          "cdna_length": 4612,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC6A1",
          "gene_hgnc_id": 11042,
          "hgvs_c": "c.1791C>T",
          "hgvs_p": "p.Ala597Ala",
          "transcript": "ENST00000645592.1",
          "protein_id": "ENSP00000496619.1",
          "transcript_support_level": null,
          "aa_start": 597,
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          "cds_start": 1791,
          "cds_end": null,
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          "cdna_start": 2112,
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          "cdna_length": 4324,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC6A1",
          "gene_hgnc_id": 11042,
          "hgvs_c": "c.1791C>T",
          "hgvs_p": "p.Ala597Ala",
          "transcript": "ENST00000645974.1",
          "protein_id": "ENSP00000496390.1",
          "transcript_support_level": null,
          "aa_start": 597,
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          "cds_start": 1791,
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          "cdna_start": 2491,
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          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
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          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
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          "exon_count": 16,
          "intron_rank": null,
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          "gene_symbol": "SLC6A1",
          "gene_hgnc_id": 11042,
          "hgvs_c": "c.1791C>T",
          "hgvs_p": "p.Ala597Ala",
          "transcript": "ENST00000646022.1",
          "protein_id": "ENSP00000494134.1",
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          "aa_start": 597,
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          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
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          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
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          "gene_symbol": "SLC6A1",
          "gene_hgnc_id": 11042,
          "hgvs_c": "c.1791C>T",
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          "transcript": "ENST00000646060.1",
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
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          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC6A1",
          "gene_hgnc_id": 11042,
          "hgvs_c": "c.1791C>T",
          "hgvs_p": "p.Ala597Ala",
          "transcript": "ENST00000646570.1",
          "protein_id": "ENSP00000496064.1",
          "transcript_support_level": null,
          "aa_start": 597,
          "aa_end": null,
          "aa_length": 599,
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          "cds_length": 1800,
          "cdna_start": 2497,
          "cdna_end": null,
          "cdna_length": 4727,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
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          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000287766.10",
          "gene_symbol": "SLC6A1",
          "hgnc_id": 11042,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AD,Unknown",
          "hgvs_c": "c.1791C>T",
          "hgvs_p": "p.Ala597Ala"
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}