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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: 16-1324523-A-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=16&pos=1324523&ref=A&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "16",
      "pos": 1324523,
      "ref": "A",
      "alt": "T",
      "effect": "intron_variant",
      "transcript": "ENST00000397514.8",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "UBE2I",
          "gene_hgnc_id": 12485,
          "hgvs_c": "c.414-207A>T",
          "hgvs_p": null,
          "transcript": "NM_003345.5",
          "protein_id": "NP_003336.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 158,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 477,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2850,
          "mane_select": "ENST00000397514.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "UBE2I",
          "gene_hgnc_id": 12485,
          "hgvs_c": "c.414-207A>T",
          "hgvs_p": null,
          "transcript": "ENST00000397514.8",
          "protein_id": "ENSP00000380649.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 158,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 477,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2850,
          "mane_select": "NM_003345.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "UBE2I",
          "gene_hgnc_id": 12485,
          "hgvs_c": "c.414-207A>T",
          "hgvs_p": null,
          "transcript": "ENST00000567074.7",
          "protein_id": "ENSP00000455893.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 158,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 477,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7031,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "UBE2I",
          "gene_hgnc_id": 12485,
          "hgvs_c": "c.*3864A>T",
          "hgvs_p": null,
          "transcript": "XM_005255540.3",
          "protein_id": "XP_005255597.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 184,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 555,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4864,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "UBE2I",
          "gene_hgnc_id": 12485,
          "hgvs_c": "c.*3864A>T",
          "hgvs_p": null,
          "transcript": "XM_011522644.3",
          "protein_id": "XP_011520946.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 184,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 555,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5121,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "UBE2I",
          "gene_hgnc_id": 12485,
          "hgvs_c": "c.*3864A>T",
          "hgvs_p": null,
          "transcript": "XM_011522645.2",
          "protein_id": "XP_011520947.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 184,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 555,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4994,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "UBE2I",
          "gene_hgnc_id": 12485,
          "hgvs_c": "c.*3864A>T",
          "hgvs_p": null,
          "transcript": "XM_047434584.1",
          "protein_id": "XP_047290540.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 184,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 555,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4846,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "UBE2I",
          "gene_hgnc_id": 12485,
          "hgvs_c": "c.*3864A>T",
          "hgvs_p": null,
          "transcript": "XM_047434585.1",
          "protein_id": "XP_047290541.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 184,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 555,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5251,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "UBE2I",
          "gene_hgnc_id": 12485,
          "hgvs_c": "c.570-207A>T",
          "hgvs_p": null,
          "transcript": "ENST00000711312.1",
          "protein_id": "ENSP00000518684.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 210,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 633,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1529,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "UBE2I",
          "gene_hgnc_id": 12485,
          "hgvs_c": "c.495-207A>T",
          "hgvs_p": null,
          "transcript": "ENST00000711324.1",
          "protein_id": "ENSP00000518689.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 185,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 558,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1231,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "UBE2I",
          "gene_hgnc_id": 12485,
          "hgvs_c": "c.224-207A>T",
          "hgvs_p": null,
          "transcript": "ENST00000711303.1",
          "protein_id": "ENSP00000518676.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 167,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 504,
          "cdna_start": null,
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          "cdna_length": 1249,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "UBE2I",
          "gene_hgnc_id": 12485,
          "hgvs_c": "c.414-207A>T",
          "hgvs_p": null,
          "transcript": "NM_194259.3",
          "protein_id": "NP_919235.1",
          "transcript_support_level": null,
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          "aa_length": 158,
          "cds_start": -4,
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          "cdna_start": null,
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        {
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          "canonical": false,
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          "strand": true,
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          "exon_rank": null,
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          "exon_count": 7,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "UBE2I",
          "gene_hgnc_id": 12485,
          "hgvs_c": "c.414-207A>T",
          "hgvs_p": null,
          "transcript": "NM_194260.3",
          "protein_id": "NP_919236.1",
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          "cds_start": -4,
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          "cdna_start": null,
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        },
        {
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          "exon_count": 7,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "UBE2I",
          "gene_hgnc_id": 12485,
          "hgvs_c": "c.414-207A>T",
          "hgvs_p": null,
          "transcript": "NM_194261.3",
          "protein_id": "NP_919237.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 158,
          "cds_start": -4,
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          "cds_length": 477,
          "cdna_start": null,
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          "mane_select": null,
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          "biotype": null,
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        },
        {
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          "canonical": false,
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          "consequences": [
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          ],
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          "intron_rank": 6,
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          "gene_symbol": "UBE2I",
          "gene_hgnc_id": 12485,
          "hgvs_c": "c.414-207A>T",
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          "transcript": "ENST00000325437.10",
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        {
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          "gene_symbol": "UBE2I",
          "gene_hgnc_id": 12485,
          "hgvs_c": "c.414-207A>T",
          "hgvs_p": null,
          "transcript": "ENST00000355803.9",
          "protein_id": "ENSP00000348056.4",
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          "cdna_start": null,
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          "feature": null
        },
        {
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          "exon_count": 8,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "UBE2I",
          "gene_hgnc_id": 12485,
          "hgvs_c": "c.414-207A>T",
          "hgvs_p": null,
          "transcript": "ENST00000397515.7",
          "protein_id": "ENSP00000380650.2",
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        {
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          "canonical": false,
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          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 8,
          "intron_rank": 7,
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          "gene_symbol": "UBE2I",
          "gene_hgnc_id": 12485,
          "hgvs_c": "c.414-207A>T",
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          "transcript": "ENST00000403747.7",
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        {
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          "gene_symbol": "UBE2I",
          "gene_hgnc_id": 12485,
          "hgvs_c": "c.414-207A>T",
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          "transcript": "ENST00000406620.6",
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        },
        {
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          ],
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          "gene_symbol": "UBE2I",
          "gene_hgnc_id": 12485,
          "hgvs_c": "c.414-207A>T",
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          "cdna_start": null,
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          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "UBE2I",
          "gene_hgnc_id": 12485,
          "hgvs_c": "c.414-207A>T",
          "hgvs_p": null,
          "transcript": "ENST00000566587.6",
          "protein_id": "ENSP00000457064.1",
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      "acmg_by_gene": [
        {
          "score": -2,
          "benign_score": 4,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000397514.8",
          "gene_symbol": "UBE2I",
          "hgnc_id": 12485,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.414-207A>T",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}