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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: 11-65659875-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=65659875&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 65659875,
      "ref": "G",
      "alt": "A",
      "effect": "intron_variant",
      "transcript": "NM_001404657.1",
      "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": 5,
          "intron_rank_end": null,
          "gene_symbol": "RELA",
          "gene_hgnc_id": 9955,
          "hgvs_c": "c.428-78C>T",
          "hgvs_p": null,
          "transcript": "NM_021975.4",
          "protein_id": "NP_068810.3",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 551,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1656,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000406246.8",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_021975.4"
        },
        {
          "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": 5,
          "intron_rank_end": null,
          "gene_symbol": "RELA",
          "gene_hgnc_id": 9955,
          "hgvs_c": "c.428-78C>T",
          "hgvs_p": null,
          "transcript": "ENST00000406246.8",
          "protein_id": "ENSP00000384273.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 551,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1656,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_021975.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000406246.8"
        },
        {
          "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": 5,
          "intron_rank_end": null,
          "gene_symbol": "RELA",
          "gene_hgnc_id": 9955,
          "hgvs_c": "c.428-87C>T",
          "hgvs_p": null,
          "transcript": "ENST00000308639.13",
          "protein_id": "ENSP00000311508.9",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 548,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1647,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000308639.13"
        },
        {
          "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": 5,
          "intron_rank_end": null,
          "gene_symbol": "RELA",
          "gene_hgnc_id": 9955,
          "hgvs_c": "c.428-78C>T",
          "hgvs_p": null,
          "transcript": "ENST00000612991.4",
          "protein_id": "ENSP00000483705.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 448,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1347,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000612991.4"
        },
        {
          "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": 10,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "RELA",
          "gene_hgnc_id": 9955,
          "hgvs_c": "c.428-78C>T",
          "hgvs_p": null,
          "transcript": "ENST00000525693.5",
          "protein_id": "ENSP00000432537.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 377,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1134,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000525693.5"
        },
        {
          "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": 5,
          "intron_rank_end": null,
          "gene_symbol": "RELA",
          "gene_hgnc_id": 9955,
          "hgvs_c": "c.461-78C>T",
          "hgvs_p": null,
          "transcript": "NM_001404657.1",
          "protein_id": "NP_001391586.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 562,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1689,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001404657.1"
        },
        {
          "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": 5,
          "intron_rank_end": null,
          "gene_symbol": "RELA",
          "gene_hgnc_id": 9955,
          "hgvs_c": "c.428-87C>T",
          "hgvs_p": null,
          "transcript": "NM_001145138.2",
          "protein_id": "NP_001138610.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 548,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1647,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001145138.2"
        },
        {
          "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": 10,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "RELA",
          "gene_hgnc_id": 9955,
          "hgvs_c": "c.401-78C>T",
          "hgvs_p": null,
          "transcript": "NM_001404658.1",
          "protein_id": "NP_001391587.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 542,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1629,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001404658.1"
        },
        {
          "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": 5,
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          "gene_symbol": "RELA",
          "gene_hgnc_id": 9955,
          "hgvs_c": "c.428-78C>T",
          "hgvs_p": null,
          "transcript": "ENST00000931854.1",
          "protein_id": "ENSP00000601913.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 541,
          "cds_start": null,
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          "cds_length": 1626,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000931854.1"
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "RELA",
          "gene_hgnc_id": 9955,
          "hgvs_c": "c.335-78C>T",
          "hgvs_p": null,
          "transcript": "NM_001404662.1",
          "protein_id": "NP_001391591.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 520,
          "cds_start": null,
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          "cds_length": 1563,
          "cdna_start": null,
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          "biotype": "protein_coding",
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        {
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          "canonical": false,
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          "hgvs_c": "c.335-78C>T",
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          "transcript": "NM_001404663.1",
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          "aa_start": null,
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          "aa_length": 520,
          "cds_start": null,
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          "cdna_start": null,
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          "mane_select": 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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          "intron_rank": 5,
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          "protein_id": "ENSP00000549016.1",
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          "gene_symbol": "RELA",
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          "hgvs_c": "c.428-78C>T",
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        {
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          "gene_symbol": "RELA",
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          "gene_symbol": "RELA",
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        {
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        {
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        {
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          "gene_symbol": "RELA",
          "gene_hgnc_id": 9955,
          "hgvs_c": "c.47-78C>T",
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          "transcript": "NM_001404661.1",
          "protein_id": "NP_001391590.1",
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          "biotype": "protein_coding",
          "feature": "NM_001404661.1"
        },
        {
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          "consequences": [
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      "clinvar_classification": "Benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "B:1",
      "phenotype_combined": "not specified",
      "pathogenicity_classification_combined": "Benign",
      "custom_annotations": null
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  "message": null
}