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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: 11-84563342-G-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=84563342&ref=G&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 84563342,
      "ref": "G",
      "alt": "T",
      "effect": "intron_variant",
      "transcript": "ENST00000376104.7",
      "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": 28,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "DLG2",
          "gene_hgnc_id": 2901,
          "hgvs_c": "c.358-28611C>A",
          "hgvs_p": null,
          "transcript": "NM_001142699.3",
          "protein_id": "NP_001136171.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 975,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2928,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7959,
          "mane_select": "ENST00000376104.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 28,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "DLG2",
          "gene_hgnc_id": 2901,
          "hgvs_c": "c.358-28611C>A",
          "hgvs_p": null,
          "transcript": "ENST00000376104.7",
          "protein_id": "ENSP00000365272.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 975,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2928,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7959,
          "mane_select": "NM_001142699.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 23,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "DLG2",
          "gene_hgnc_id": 2901,
          "hgvs_c": "c.43-28611C>A",
          "hgvs_p": null,
          "transcript": "ENST00000398309.6",
          "protein_id": "ENSP00000381355.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 870,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2613,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7890,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 23,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "DLG2",
          "gene_hgnc_id": 2901,
          "hgvs_c": "c.43-28611C>A",
          "hgvs_p": null,
          "transcript": "ENST00000532653.5",
          "protein_id": "ENSP00000435849.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 852,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2559,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2891,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "DLG2",
          "gene_hgnc_id": 2901,
          "hgvs_c": "n.321-28611C>A",
          "hgvs_p": null,
          "transcript": "ENST00000529111.5",
          "protein_id": null,
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3926,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 28,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "DLG2",
          "gene_hgnc_id": 2901,
          "hgvs_c": "c.469-28611C>A",
          "hgvs_p": null,
          "transcript": "ENST00000650630.1",
          "protein_id": "ENSP00000497771.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1012,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3039,
          "cdna_start": null,
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          "cdna_length": 5127,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 27,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "DLG2",
          "gene_hgnc_id": 2901,
          "hgvs_c": "c.394-28611C>A",
          "hgvs_p": null,
          "transcript": "NM_001351274.2",
          "protein_id": "NP_001338203.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 969,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2910,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8537,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 27,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "DLG2",
          "gene_hgnc_id": 2901,
          "hgvs_c": "c.394-28611C>A",
          "hgvs_p": null,
          "transcript": "ENST00000706226.1",
          "protein_id": "ENSP00000516284.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 969,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2910,
          "cdna_start": null,
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          "cdna_length": 3626,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 26,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "DLG2",
          "gene_hgnc_id": 2901,
          "hgvs_c": "c.394-28614C>A",
          "hgvs_p": null,
          "transcript": "NM_001351275.2",
          "protein_id": "NP_001338204.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
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          "biotype": null,
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        },
        {
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          "consequences": [
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          "exon_rank": null,
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          "exon_count": 26,
          "intron_rank": 4,
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          "gene_symbol": "DLG2",
          "gene_hgnc_id": 2901,
          "hgvs_c": "c.394-28614C>A",
          "hgvs_p": null,
          "transcript": "ENST00000706233.1",
          "protein_id": "ENSP00000516288.1",
          "transcript_support_level": null,
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          "cds_start": -4,
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          "gene_symbol": "DLG2",
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      "clinvar_disease": "",
      "clinvar_classification": "",
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  "message": null
}