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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: 4-2829995-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=4&pos=2829995&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "4",
      "pos": 2829995,
      "ref": "T",
      "alt": "C",
      "effect": "synonymous_variant",
      "transcript": "NM_001145856.2",
      "consequences": [
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SH3BP2",
          "gene_hgnc_id": 10825,
          "hgvs_c": "c.1089T>C",
          "hgvs_p": "p.Ala363Ala",
          "transcript": "NM_001122681.2",
          "protein_id": "NP_001116153.1",
          "transcript_support_level": null,
          "aa_start": 363,
          "aa_end": null,
          "aa_length": 561,
          "cds_start": 1089,
          "cds_end": null,
          "cds_length": 1686,
          "cdna_start": 1147,
          "cdna_end": null,
          "cdna_length": 9006,
          "mane_select": "ENST00000503393.8",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001122681.2"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SH3BP2",
          "gene_hgnc_id": 10825,
          "hgvs_c": "c.1089T>C",
          "hgvs_p": "p.Ala363Ala",
          "transcript": "ENST00000503393.8",
          "protein_id": "ENSP00000422168.3",
          "transcript_support_level": 1,
          "aa_start": 363,
          "aa_end": null,
          "aa_length": 561,
          "cds_start": 1089,
          "cds_end": null,
          "cds_length": 1686,
          "cdna_start": 1147,
          "cdna_end": null,
          "cdna_length": 9006,
          "mane_select": "NM_001122681.2",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000503393.8"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SH3BP2",
          "gene_hgnc_id": 10825,
          "hgvs_c": "c.1260T>C",
          "hgvs_p": "p.Ala420Ala",
          "transcript": "ENST00000511747.6",
          "protein_id": "ENSP00000424846.2",
          "transcript_support_level": 1,
          "aa_start": 420,
          "aa_end": null,
          "aa_length": 618,
          "cds_start": 1260,
          "cds_end": null,
          "cds_length": 1857,
          "cdna_start": 1299,
          "cdna_end": null,
          "cdna_length": 2351,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000511747.6"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SH3BP2",
          "gene_hgnc_id": 10825,
          "hgvs_c": "n.1350T>C",
          "hgvs_p": null,
          "transcript": "ENST00000356331.10",
          "protein_id": null,
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 9211,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "retained_intron",
          "feature": "ENST00000356331.10"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SH3BP2",
          "gene_hgnc_id": 10825,
          "hgvs_c": "c.1260T>C",
          "hgvs_p": "p.Ala420Ala",
          "transcript": "NM_001145856.2",
          "protein_id": "NP_001139328.1",
          "transcript_support_level": null,
          "aa_start": 420,
          "aa_end": null,
          "aa_length": 618,
          "cds_start": 1260,
          "cds_end": null,
          "cds_length": 1857,
          "cdna_start": 1314,
          "cdna_end": null,
          "cdna_length": 9173,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001145856.2"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SH3BP2",
          "gene_hgnc_id": 10825,
          "hgvs_c": "c.1260T>C",
          "hgvs_p": "p.Ala420Ala",
          "transcript": "ENST00000932791.1",
          "protein_id": "ENSP00000602850.1",
          "transcript_support_level": null,
          "aa_start": 420,
          "aa_end": null,
          "aa_length": 618,
          "cds_start": 1260,
          "cds_end": null,
          "cds_length": 1857,
          "cdna_start": 1483,
          "cdna_end": null,
          "cdna_length": 5285,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000932791.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SH3BP2",
          "gene_hgnc_id": 10825,
          "hgvs_c": "c.1173T>C",
          "hgvs_p": "p.Ala391Ala",
          "transcript": "NM_001145855.2",
          "protein_id": "NP_001139327.1",
          "transcript_support_level": null,
          "aa_start": 391,
          "aa_end": null,
          "aa_length": 589,
          "cds_start": 1173,
          "cds_end": null,
          "cds_length": 1770,
          "cdna_start": 1280,
          "cdna_end": null,
          "cdna_length": 9139,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001145855.2"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SH3BP2",
          "gene_hgnc_id": 10825,
          "hgvs_c": "c.1173T>C",
          "hgvs_p": "p.Ala391Ala",
          "transcript": "ENST00000435136.8",
          "protein_id": "ENSP00000403231.3",
          "transcript_support_level": 2,
          "aa_start": 391,
          "aa_end": null,
          "aa_length": 589,
          "cds_start": 1173,
          "cds_end": null,
          "cds_length": 1770,
          "cdna_start": 1280,
          "cdna_end": null,
          "cdna_length": 9139,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000435136.8"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SH3BP2",
          "gene_hgnc_id": 10825,
          "hgvs_c": "c.1089T>C",
          "hgvs_p": "p.Ala363Ala",
          "transcript": "ENST00000893561.1",
          "protein_id": "ENSP00000563620.1",
          "transcript_support_level": null,
          "aa_start": 363,
          "aa_end": null,
          "aa_length": 573,
          "cds_start": 1089,
          "cds_end": null,
          "cds_length": 1722,
          "cdna_start": 1147,
          "cdna_end": null,
          "cdna_length": 2232,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000893561.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SH3BP2",
          "gene_hgnc_id": 10825,
          "hgvs_c": "c.1089T>C",
          "hgvs_p": "p.Ala363Ala",
          "transcript": "NM_003023.4",
          "protein_id": "NP_003014.3",
          "transcript_support_level": null,
          "aa_start": 363,
          "aa_end": null,
          "aa_length": 561,
          "cds_start": 1089,
          "cds_end": null,
          "cds_length": 1686,
          "cdna_start": 1350,
          "cdna_end": null,
          "cdna_length": 9209,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_003023.4"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SH3BP2",
          "gene_hgnc_id": 10825,
          "hgvs_c": "c.1089T>C",
          "hgvs_p": "p.Ala363Ala",
          "transcript": "ENST00000502260.6",
          "protein_id": "ENSP00000425537.2",
          "transcript_support_level": 3,
          "aa_start": 363,
          "aa_end": null,
          "aa_length": 561,
          "cds_start": 1089,
          "cds_end": null,
          "cds_length": 1686,
          "cdna_start": 1388,
          "cdna_end": null,
          "cdna_length": 9247,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000502260.6"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SH3BP2",
          "gene_hgnc_id": 10825,
          "hgvs_c": "c.1089T>C",
          "hgvs_p": "p.Ala363Ala",
          "transcript": "ENST00000503219.7",
          "protein_id": "ENSP00000422796.2",
          "transcript_support_level": 4,
          "aa_start": 363,
          "aa_end": null,
          "aa_length": 561,
          "cds_start": 1089,
          "cds_end": null,
          "cds_length": 1686,
          "cdna_start": 1212,
          "cdna_end": null,
          "cdna_length": 9073,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000503219.7"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SH3BP2",
          "gene_hgnc_id": 10825,
          "hgvs_c": "c.1089T>C",
          "hgvs_p": "p.Ala363Ala",
          "transcript": "ENST00000504294.6",
          "protein_id": "ENSP00000423275.2",
          "transcript_support_level": 5,
          "aa_start": 363,
          "aa_end": null,
          "aa_length": 561,
          "cds_start": 1089,
          "cds_end": null,
          "cds_length": 1686,
          "cdna_start": 1129,
          "cdna_end": null,
          "cdna_length": 8988,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000504294.6"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SH3BP2",
          "gene_hgnc_id": 10825,
          "hgvs_c": "c.1089T>C",
          "hgvs_p": "p.Ala363Ala",
          "transcript": "ENST00000508385.6",
          "protein_id": "ENSP00000424917.2",
          "transcript_support_level": 3,
          "aa_start": 363,
          "aa_end": null,
          "aa_length": 561,
          "cds_start": 1089,
          "cds_end": null,
          "cds_length": 1686,
          "cdna_start": 1401,
          "cdna_end": null,
          "cdna_length": 9260,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000508385.6"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SH3BP2",
          "gene_hgnc_id": 10825,
          "hgvs_c": "c.1089T>C",
          "hgvs_p": "p.Ala363Ala",
          "transcript": "ENST00000512014.6",
          "protein_id": "ENSP00000424105.2",
          "transcript_support_level": 3,
          "aa_start": 363,
          "aa_end": null,
          "aa_length": 561,
          "cds_start": 1089,
          "cds_end": null,
          "cds_length": 1686,
          "cdna_start": 1195,
          "cdna_end": null,
          "cdna_length": 9054,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000512014.6"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SH3BP2",
          "gene_hgnc_id": 10825,
          "hgvs_c": "c.1089T>C",
          "hgvs_p": "p.Ala363Ala",
          "transcript": "ENST00000513095.6",
          "protein_id": "ENSP00000423823.2",
          "transcript_support_level": 4,
          "aa_start": 363,
          "aa_end": null,
          "aa_length": 561,
          "cds_start": 1089,
          "cds_end": null,
          "cds_length": 1686,
          "cdna_start": 1288,
          "cdna_end": null,
          "cdna_length": 9147,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000513095.6"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SH3BP2",
          "gene_hgnc_id": 10825,
          "hgvs_c": "c.1089T>C",
          "hgvs_p": "p.Ala363Ala",
          "transcript": "ENST00000893545.1",
          "protein_id": "ENSP00000563604.1",
          "transcript_support_level": null,
          "aa_start": 363,
          "aa_end": null,
          "aa_length": 561,
          "cds_start": 1089,
          "cds_end": null,
          "cds_length": 1686,
          "cdna_start": 1337,
          "cdna_end": null,
          "cdna_length": 5138,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000893545.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SH3BP2",
          "gene_hgnc_id": 10825,
          "hgvs_c": "c.1089T>C",
          "hgvs_p": "p.Ala363Ala",
          "transcript": "ENST00000893546.1",
          "protein_id": "ENSP00000563605.1",
          "transcript_support_level": null,
          "aa_start": 363,
          "aa_end": null,
          "aa_length": 561,
          "cds_start": 1089,
          "cds_end": null,
          "cds_length": 1686,
          "cdna_start": 1305,
          "cdna_end": null,
          "cdna_length": 2361,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000893546.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SH3BP2",
          "gene_hgnc_id": 10825,
          "hgvs_c": "c.1089T>C",
          "hgvs_p": "p.Ala363Ala",
          "transcript": "ENST00000893548.1",
          "protein_id": "ENSP00000563607.1",
          "transcript_support_level": null,
          "aa_start": 363,
          "aa_end": null,
          "aa_length": 561,
          "cds_start": 1089,
          "cds_end": null,
          "cds_length": 1686,
          "cdna_start": 1590,
          "cdna_end": null,
          "cdna_length": 2642,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000893548.1"
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SH3BP2",
          "gene_hgnc_id": 10825,
          "hgvs_c": "c.1089T>C",
          "hgvs_p": "p.Ala363Ala",
          "transcript": "ENST00000893549.1",
          "protein_id": "ENSP00000563608.1",
          "transcript_support_level": null,
          "aa_start": 363,
          "aa_end": null,
          "aa_length": 561,
          "cds_start": 1089,
          "cds_end": null,
          "cds_length": 1686,
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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.