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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: 8-143924194-AG-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=8&pos=143924194&ref=AG&alt=A&genome=hg38&allGenes=true"API Response
json
{
  "variants": [
    {
      "chr": "8",
      "pos": 143924194,
      "ref": "AG",
      "alt": "A",
      "effect": "frameshift_variant",
      "transcript": "ENST00000345136.8",
      "consequences": [
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.5734delC",
          "hgvs_p": "p.Leu1912fs",
          "transcript": "NM_201384.3",
          "protein_id": "NP_958786.1",
          "transcript_support_level": null,
          "aa_start": 1912,
          "aa_end": null,
          "aa_length": 4547,
          "cds_start": 5734,
          "cds_end": null,
          "cds_length": 13644,
          "cdna_start": 5870,
          "cdna_end": null,
          "cdna_length": 14804,
          "mane_select": "ENST00000345136.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.5734delC",
          "hgvs_p": "p.Leu1912fs",
          "transcript": "ENST00000345136.8",
          "protein_id": "ENSP00000344848.3",
          "transcript_support_level": 1,
          "aa_start": 1912,
          "aa_end": null,
          "aa_length": 4547,
          "cds_start": 5734,
          "cds_end": null,
          "cds_length": 13644,
          "cdna_start": 5870,
          "cdna_end": null,
          "cdna_length": 14804,
          "mane_select": "NM_201384.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.5692delC",
          "hgvs_p": "p.Leu1898fs",
          "transcript": "NM_201378.4",
          "protein_id": "NP_958780.1",
          "transcript_support_level": null,
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          "aa_end": null,
          "aa_length": 4533,
          "cds_start": 5692,
          "cds_end": null,
          "cds_length": 13602,
          "cdna_start": 5749,
          "cdna_end": null,
          "cdna_length": 14683,
          "mane_select": null,
          "mane_plus": "ENST00000356346.7",
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.5692delC",
          "hgvs_p": "p.Leu1898fs",
          "transcript": "ENST00000356346.7",
          "protein_id": "ENSP00000348702.3",
          "transcript_support_level": 1,
          "aa_start": 1898,
          "aa_end": null,
          "aa_length": 4533,
          "cds_start": 5692,
          "cds_end": null,
          "cds_length": 13602,
          "cdna_start": 5749,
          "cdna_end": null,
          "cdna_length": 14683,
          "mane_select": null,
          "mane_plus": "NM_201378.4",
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.6145delC",
          "hgvs_p": "p.Leu2049fs",
          "transcript": "ENST00000322810.8",
          "protein_id": "ENSP00000323856.4",
          "transcript_support_level": 1,
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          "cdna_start": 6315,
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          "cdna_length": 15249,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
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          "hgvs_c": "c.5815delC",
          "hgvs_p": "p.Leu1939fs",
          "transcript": "ENST00000436759.6",
          "protein_id": "ENSP00000388180.2",
          "transcript_support_level": 1,
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        {
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          "strand": false,
          "consequences": [
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          "exon_rank": 31,
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          "exon_count": 32,
          "intron_rank": null,
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          "gene_symbol": "PLEC",
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          "hgvs_c": "c.5746delC",
          "hgvs_p": "p.Leu1916fs",
          "transcript": "ENST00000357649.6",
          "protein_id": "ENSP00000350277.2",
          "transcript_support_level": 1,
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        {
          "aa_ref": "L",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
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          "gene_symbol": "PLEC",
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          "hgvs_c": "c.5734delC",
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          "transcript": "ENST00000354589.7",
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      "clinvar_review_status": "no assertion criteria provided",
      "clinvar_submissions_summary": "null",
      "phenotype_combined": "Epidermolysis bullosa simplex 5B, with muscular dystrophy",
      "pathogenicity_classification_combined": "Pathogenic",
      "custom_annotations": null
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