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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: 2-151496969-ACTCT-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=151496969&ref=ACTCT&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 151496969,
      "ref": "ACTCT",
      "alt": "A",
      "effect": "frameshift_variant",
      "transcript": "ENST00000397345.8",
      "consequences": [
        {
          "aa_ref": "RV",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 172,
          "exon_rank_end": null,
          "exon_count": 182,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NEB",
          "gene_hgnc_id": 7720,
          "hgvs_c": "c.24361_24364delAGAG",
          "hgvs_p": "p.Arg8121fs",
          "transcript": "NM_001164507.2",
          "protein_id": "NP_001157979.2",
          "transcript_support_level": null,
          "aa_start": 8121,
          "aa_end": null,
          "aa_length": 8525,
          "cds_start": 24361,
          "cds_end": null,
          "cds_length": 25578,
          "cdna_start": 24556,
          "cdna_end": null,
          "cdna_length": 26191,
          "mane_select": null,
          "mane_plus": "ENST00000427231.7",
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "RV",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 172,
          "exon_rank_end": null,
          "exon_count": 182,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NEB",
          "gene_hgnc_id": 7720,
          "hgvs_c": "c.24361_24364delAGAG",
          "hgvs_p": "p.Arg8121fs",
          "transcript": "NM_001164508.2",
          "protein_id": "NP_001157980.2",
          "transcript_support_level": null,
          "aa_start": 8121,
          "aa_end": null,
          "aa_length": 8525,
          "cds_start": 24361,
          "cds_end": null,
          "cds_length": 25578,
          "cdna_start": 24556,
          "cdna_end": null,
          "cdna_length": 26191,
          "mane_select": "ENST00000397345.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "RV",
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 172,
          "exon_rank_end": null,
          "exon_count": 182,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NEB",
          "gene_hgnc_id": 7720,
          "hgvs_c": "c.24361_24364delAGAG",
          "hgvs_p": "p.Arg8121fs",
          "transcript": "ENST00000397345.8",
          "protein_id": "ENSP00000380505.3",
          "transcript_support_level": 5,
          "aa_start": 8121,
          "aa_end": null,
          "aa_length": 8525,
          "cds_start": 24361,
          "cds_end": null,
          "cds_length": 25578,
          "cdna_start": 24556,
          "cdna_end": null,
          "cdna_length": 26191,
          "mane_select": "NM_001164508.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "RV",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 172,
          "exon_rank_end": null,
          "exon_count": 182,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NEB",
          "gene_hgnc_id": 7720,
          "hgvs_c": "c.24361_24364delAGAG",
          "hgvs_p": "p.Arg8121fs",
          "transcript": "ENST00000427231.7",
          "protein_id": "ENSP00000416578.2",
          "transcript_support_level": 5,
          "aa_start": 8121,
          "aa_end": null,
          "aa_length": 8525,
          "cds_start": 24361,
          "cds_end": null,
          "cds_length": 25578,
          "cdna_start": 24556,
          "cdna_end": null,
          "cdna_length": 26191,
          "mane_select": null,
          "mane_plus": "NM_001164507.2",
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "RIF1",
          "gene_hgnc_id": 23207,
          "hgvs_c": "n.579-813_579-810delTCTC",
          "hgvs_p": null,
          "transcript": "ENST00000457745.1",
          "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": 1006,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "RV",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 173,
          "exon_rank_end": null,
          "exon_count": 183,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NEB",
          "gene_hgnc_id": 7720,
          "hgvs_c": "c.24466_24469delAGAG",
          "hgvs_p": "p.Arg8156fs",
          "transcript": "NM_001271208.2",
          "protein_id": "NP_001258137.2",
          "transcript_support_level": null,
          "aa_start": 8156,
          "aa_end": null,
          "aa_length": 8560,
          "cds_start": 24466,
          "cds_end": null,
          "cds_length": 25683,
          "cdna_start": 24661,
          "cdna_end": null,
          "cdna_length": 26296,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "RV",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NEB",
          "gene_hgnc_id": 7720,
          "hgvs_c": "c.958_961delAGAG",
          "hgvs_p": "p.Arg320fs",
          "transcript": "ENST00000688578.1",
          "protein_id": "ENSP00000509628.1",
          "transcript_support_level": null,
          "aa_start": 320,
          "aa_end": null,
          "aa_length": 724,
          "cds_start": 958,
          "cds_end": null,
          "cds_length": 2175,
          "cdna_start": 963,
          "cdna_end": null,
          "cdna_length": 2177,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "RV",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NEB",
          "gene_hgnc_id": 7720,
          "hgvs_c": "c.760_763delAGAG",
          "hgvs_p": "p.Arg254fs",
          "transcript": "ENST00000397337.6",
          "protein_id": "ENSP00000380498.2",
          "transcript_support_level": 5,
          "aa_start": 254,
          "aa_end": null,
          "aa_length": 658,
          "cds_start": 760,
          "cds_end": null,
          "cds_length": 1977,
          "cdna_start": 765,
          "cdna_end": null,
          "cdna_length": 2400,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "RV",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NEB",
          "gene_hgnc_id": 7720,
          "hgvs_c": "c.796_799delAGAG",
          "hgvs_p": "p.Arg266fs",
          "transcript": "ENST00000421461.6",
          "protein_id": "ENSP00000408570.2",
          "transcript_support_level": 5,
          "aa_start": 266,
          "aa_end": null,
          "aa_length": 399,
          "cds_start": 796,
          "cds_end": null,
          "cds_length": 1200,
          "cdna_start": 800,
          "cdna_end": null,
          "cdna_length": 1201,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "RV",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NEB",
          "gene_hgnc_id": 7720,
          "hgvs_c": "c.670_673delAGAG",
          "hgvs_p": "p.Arg224fs",
          "transcript": "ENST00000424585.1",
          "protein_id": "ENSP00000404876.1",
          "transcript_support_level": 3,
          "aa_start": 224,
          "aa_end": null,
          "aa_length": 254,
          "cds_start": 670,
          "cds_end": null,
          "cds_length": 766,
          "cdna_start": 673,
          "cdna_end": null,
          "cdna_length": 766,
          "mane_select": null,
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        },
        {
          "aa_ref": "RV",
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          "canonical": false,
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          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 171,
          "exon_rank_end": null,
          "exon_count": 181,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NEB",
          "gene_hgnc_id": 7720,
          "hgvs_c": "c.24268_24271delAGAG",
          "hgvs_p": "p.Arg8090fs",
          "transcript": "XM_005246590.3",
          "protein_id": "XP_005246647.1",
          "transcript_support_level": null,
          "aa_start": 8090,
          "aa_end": null,
          "aa_length": 8494,
          "cds_start": 24268,
          "cds_end": null,
          "cds_length": 25485,
          "cdna_start": 24463,
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          "cdna_length": 26098,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "RV",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 171,
          "exon_rank_end": null,
          "exon_count": 181,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NEB",
          "gene_hgnc_id": 7720,
          "hgvs_c": "c.24268_24271delAGAG",
          "hgvs_p": "p.Arg8090fs",
          "transcript": "XM_005246591.3",
          "protein_id": "XP_005246648.1",
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          "cds_start": 24268,
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        },
        {
          "aa_ref": "RV",
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 172,
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          "exon_count": 181,
          "intron_rank": null,
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          "gene_symbol": "NEB",
          "gene_hgnc_id": 7720,
          "hgvs_c": "c.24361_24364delAGAG",
          "hgvs_p": "p.Arg8121fs",
          "transcript": "XM_005246593.3",
          "protein_id": "XP_005246650.1",
          "transcript_support_level": null,
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        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 171,
          "exon_rank_end": null,
          "exon_count": 181,
          "intron_rank": null,
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          "gene_symbol": "NEB",
          "gene_hgnc_id": 7720,
          "hgvs_c": "c.24268_24271delAGAG",
          "hgvs_p": "p.Arg8090fs",
          "transcript": "XM_005246594.3",
          "protein_id": "XP_005246651.1",
          "transcript_support_level": null,
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        },
        {
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          ],
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          "intron_rank": null,
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          "gene_symbol": "NEB",
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          "hgvs_c": "c.24250_24253delAGAG",
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          "transcript": "XM_017004177.2",
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          "biotype": null,
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        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 170,
          "exon_rank_end": null,
          "exon_count": 180,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NEB",
          "gene_hgnc_id": 7720,
          "hgvs_c": "c.24175_24178delAGAG",
          "hgvs_p": "p.Arg8059fs",
          "transcript": "XM_005246596.3",
          "protein_id": "XP_005246653.1",
          "transcript_support_level": null,
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          "mane_select": null,
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        },
        {
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          ],
          "exon_rank": 172,
          "exon_rank_end": null,
          "exon_count": 180,
          "intron_rank": null,
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          "gene_symbol": "NEB",
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          "hgvs_c": "c.24361_24364delAGAG",
          "hgvs_p": "p.Arg8121fs",
          "transcript": "XM_005246598.3",
          "protein_id": "XP_005246655.1",
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        },
        {
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          "exon_count": 180,
          "intron_rank": null,
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        },
        {
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          ],
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          "exon_rank_end": null,
          "exon_count": 180,
          "intron_rank": null,
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          "gene_symbol": "NEB",
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          "transcript": "XM_047444477.1",
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        },
        {
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 169,
          "exon_rank_end": null,
          "exon_count": 179,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "NEB",
          "gene_hgnc_id": 7720,
          "hgvs_c": "c.24082_24085delAGAG",
          "hgvs_p": "p.Arg8028fs",
          "transcript": "XM_005246599.3",
          "protein_id": "XP_005246656.1",
          "transcript_support_level": null,
          "aa_start": 8028,
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          "aa_length": 8432,
          "cds_start": 24082,
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          "cds_length": 25299,
          "cdna_start": 24277,
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          "cdna_length": 25912,
          "mane_select": null,
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        },
        {
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          "aa_alt": null,
          "canonical": false,
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          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 168,
          "exon_rank_end": null,
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      "clinvar_classification": "Pathogenic/Likely pathogenic",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "P:1 LP:1",
      "phenotype_combined": "Arthrogryposis multiplex congenita 6;Nemaline myopathy 2|Nemaline myopathy 2",
      "pathogenicity_classification_combined": "Pathogenic/Likely pathogenic",
      "custom_annotations": null
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  "message": null
}