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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: 13-46055860-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=13&pos=46055860&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "13",
      "pos": 46055860,
      "ref": "C",
      "alt": "A",
      "effect": "intron_variant",
      "transcript": "NM_001872.5",
      "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": 11,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "CPB2",
          "gene_hgnc_id": 2300,
          "hgvs_c": "c.1000-11G>T",
          "hgvs_p": null,
          "transcript": "NM_001872.5",
          "protein_id": "NP_001863.3",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 423,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1272,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000181383.10",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001872.5"
        },
        {
          "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": 11,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "CPB2",
          "gene_hgnc_id": 2300,
          "hgvs_c": "c.1000-11G>T",
          "hgvs_p": null,
          "transcript": "ENST00000181383.10",
          "protein_id": "ENSP00000181383.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 423,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1272,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_001872.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000181383.10"
        },
        {
          "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": 11,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "CPB2",
          "gene_hgnc_id": 2300,
          "hgvs_c": "c.1102-11G>T",
          "hgvs_p": null,
          "transcript": "ENST00000882332.1",
          "protein_id": "ENSP00000552391.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 457,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1374,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000882332.1"
        },
        {
          "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": 11,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "CPB2",
          "gene_hgnc_id": 2300,
          "hgvs_c": "c.1048-11G>T",
          "hgvs_p": null,
          "transcript": "ENST00000882315.1",
          "protein_id": "ENSP00000552374.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 439,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1320,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000882315.1"
        },
        {
          "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": 12,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "CPB2",
          "gene_hgnc_id": 2300,
          "hgvs_c": "c.1042-11G>T",
          "hgvs_p": null,
          "transcript": "ENST00000882319.1",
          "protein_id": "ENSP00000552378.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 437,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1314,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000882319.1"
        },
        {
          "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": 11,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "CPB2",
          "gene_hgnc_id": 2300,
          "hgvs_c": "c.1024-11G>T",
          "hgvs_p": null,
          "transcript": "ENST00000882325.1",
          "protein_id": "ENSP00000552384.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 431,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1296,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000882325.1"
        },
        {
          "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": 11,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "CPB2",
          "gene_hgnc_id": 2300,
          "hgvs_c": "c.1003-11G>T",
          "hgvs_p": null,
          "transcript": "ENST00000882322.1",
          "protein_id": "ENSP00000552381.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 424,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1275,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000882322.1"
        },
        {
          "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": 11,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "CPB2",
          "gene_hgnc_id": 2300,
          "hgvs_c": "c.994-11G>T",
          "hgvs_p": null,
          "transcript": "ENST00000882327.1",
          "protein_id": "ENSP00000552386.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 421,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1266,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000882327.1"
        },
        {
          "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": 11,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "CPB2",
          "gene_hgnc_id": 2300,
          "hgvs_c": "c.1000-11G>T",
          "hgvs_p": null,
          "transcript": "ENST00000882328.1",
          "protein_id": "ENSP00000552387.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 421,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1266,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000882328.1"
        },
        {
          "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": 11,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "CPB2",
          "gene_hgnc_id": 2300,
          "hgvs_c": "c.985-11G>T",
          "hgvs_p": null,
          "transcript": "ENST00000882320.1",
          "protein_id": "ENSP00000552379.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 418,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1257,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000882320.1"
        },
        {
          "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": 8,
          "intron_rank_end": null,
          "gene_symbol": "CPB2",
          "gene_hgnc_id": 2300,
          "hgvs_c": "c.937-11G>T",
          "hgvs_p": null,
          "transcript": "ENST00000882326.1",
          "protein_id": "ENSP00000552385.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 402,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1209,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000882326.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 8,
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          "gene_symbol": "CPB2",
          "gene_hgnc_id": 2300,
          "hgvs_c": "c.913-11G>T",
          "hgvs_p": null,
          "transcript": "ENST00000882333.1",
          "protein_id": "ENSP00000552392.1",
          "transcript_support_level": null,
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          "aa_end": null,
          "aa_length": 394,
          "cds_start": null,
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          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": null,
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          "consequences": [
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          ],
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          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "CPB2",
          "gene_hgnc_id": 2300,
          "hgvs_c": "c.898-11G>T",
          "hgvs_p": null,
          "transcript": "ENST00000882317.1",
          "protein_id": "ENSP00000552376.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 389,
          "cds_start": null,
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          "cdna_start": null,
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        },
        {
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          "canonical": false,
          "protein_coding": true,
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          "exon_count": 10,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "CPB2",
          "gene_hgnc_id": 2300,
          "hgvs_c": "c.889-11G>T",
          "hgvs_p": null,
          "transcript": "NM_001278541.2",
          "protein_id": "NP_001265470.1",
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          "aa_start": null,
          "aa_end": null,
          "aa_length": 386,
          "cds_start": null,
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          "biotype": "protein_coding",
          "feature": "NM_001278541.2"
        },
        {
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          "gene_symbol": "CPB2",
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          "hgvs_c": "c.889-11G>T",
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          "transcript": "ENST00000439329.5",
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          "aa_start": null,
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          "cdna_start": null,
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          "biotype": "protein_coding",
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        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          "exon_count": 10,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "CPB2",
          "gene_hgnc_id": 2300,
          "hgvs_c": "c.883-11G>T",
          "hgvs_p": null,
          "transcript": "ENST00000882334.1",
          "protein_id": "ENSP00000552393.1",
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          "aa_length": 384,
          "cds_start": null,
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          "feature": "ENST00000882334.1"
        },
        {
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          ],
          "exon_rank": null,
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          "exon_count": 10,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "CPB2",
          "gene_hgnc_id": 2300,
          "hgvs_c": "c.874-11G>T",
          "hgvs_p": null,
          "transcript": "ENST00000882331.1",
          "protein_id": "ENSP00000552390.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 381,
          "cds_start": null,
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          "cds_length": 1146,
          "cdna_start": null,
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          "intron_rank": 7,
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          "gene_symbol": "CPB2",
          "gene_hgnc_id": 2300,
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          "transcript": "ENST00000882323.1",
          "protein_id": "ENSP00000552382.1",
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        },
        {
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          "consequences": [
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          ],
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          "intron_rank": 7,
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          "gene_symbol": "CPB2",
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          "hgvs_c": "c.793-11G>T",
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          "transcript": "ENST00000882321.1",
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          "biotype": "protein_coding",
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        },
        {
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          "canonical": false,
          "protein_coding": true,
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          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 9,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "CPB2",
          "gene_hgnc_id": 2300,
          "hgvs_c": "c.787-11G>T",
          "hgvs_p": null,
          "transcript": "ENST00000882324.1",
          "protein_id": "ENSP00000552383.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 352,
          "cds_start": null,
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          "cds_length": 1059,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000882324.1"
        },
        {
          "aa_ref": null,
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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      "splice_prediction_selected": "Benign",
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      "spliceai_max_score": 0,
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      "acmg_classification": "Benign",
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      "acmg_by_gene": [
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          "verdict": "Benign",
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          "gene_symbol": "CPB2-AS1",
          "hgnc_id": 39898,
          "effects": [
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          "inheritance_mode": "",
          "hgvs_c": "n.165+2895C>A",
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      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}