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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: 12-96010211-T-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=96010211&ref=T&alt=A&genome=hg38&allGenes=true"API Response
json
{
  "variants": [
    {
      "chr": "12",
      "pos": 96010211,
      "ref": "T",
      "alt": "A",
      "effect": "intron_variant",
      "transcript": "ENST00000228740.7",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LTA4H",
          "gene_hgnc_id": 6710,
          "hgvs_c": "n.1048A>T",
          "hgvs_p": null,
          "transcript": "ENST00000537111.6",
          "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": 1881,
          "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": 19,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "LTA4H",
          "gene_hgnc_id": 6710,
          "hgvs_c": "c.1380-1063A>T",
          "hgvs_p": null,
          "transcript": "NM_000895.3",
          "protein_id": "NP_000886.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 611,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1836,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2140,
          "mane_select": "ENST00000228740.7",
          "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": 19,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "LTA4H",
          "gene_hgnc_id": 6710,
          "hgvs_c": "c.1380-1063A>T",
          "hgvs_p": null,
          "transcript": "ENST00000228740.7",
          "protein_id": "ENSP00000228740.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 611,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1836,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2140,
          "mane_select": "NM_000895.3",
          "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": 19,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "LTA4H",
          "gene_hgnc_id": 6710,
          "hgvs_c": "c.1308-1063A>T",
          "hgvs_p": null,
          "transcript": "ENST00000552789.5",
          "protein_id": "ENSP00000449958.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 587,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1764,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2025,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LTA4H",
          "gene_hgnc_id": 6710,
          "hgvs_c": "n.4434A>T",
          "hgvs_p": null,
          "transcript": "ENST00000553041.5",
          "protein_id": null,
          "transcript_support_level": 2,
          "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": 6109,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LOC102723340",
          "gene_hgnc_id": null,
          "hgvs_c": "n.570T>A",
          "hgvs_p": null,
          "transcript": "XR_001749275.3",
          "protein_id": null,
          "transcript_support_level": null,
          "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": 2063,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LOC102723340",
          "gene_hgnc_id": null,
          "hgvs_c": "n.339T>A",
          "hgvs_p": null,
          "transcript": "XR_002957423.2",
          "protein_id": null,
          "transcript_support_level": null,
          "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": 1832,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LOC102723340",
          "gene_hgnc_id": null,
          "hgvs_c": "n.400T>A",
          "hgvs_p": null,
          "transcript": "XR_002957424.2",
          "protein_id": null,
          "transcript_support_level": null,
          "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": 1893,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LOC102723340",
          "gene_hgnc_id": null,
          "hgvs_c": "n.991T>A",
          "hgvs_p": null,
          "transcript": "XR_945236.4",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 2484,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LOC102723340",
          "gene_hgnc_id": null,
          "hgvs_c": "n.667T>A",
          "hgvs_p": null,
          "transcript": "XR_945237.4",
          "protein_id": null,
          "transcript_support_level": null,
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          "mane_select": null,
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          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 19,
          "intron_rank": 14,
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          "gene_symbol": "LTA4H",
          "gene_hgnc_id": 6710,
          "hgvs_c": "c.1308-1063A>T",
          "hgvs_p": null,
          "transcript": "NM_001256643.1",
          "protein_id": "NP_001243572.1",
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        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 18,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "LTA4H",
          "gene_hgnc_id": 6710,
          "hgvs_c": "c.1380-1063A>T",
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          "transcript": "NM_001414263.1",
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        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
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          "exon_count": 18,
          "intron_rank": 13,
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          "gene_symbol": "LTA4H",
          "gene_hgnc_id": 6710,
          "hgvs_c": "c.1275-1063A>T",
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          "consequences": [
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          ],
          "exon_rank": null,
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          "intron_rank": 14,
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          "gene_symbol": "LTA4H",
          "gene_hgnc_id": 6710,
          "hgvs_c": "c.1380-1063A>T",
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          "transcript": "NM_001414265.1",
          "protein_id": "NP_001401194.1",
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        },
        {
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          ],
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          "intron_rank": 14,
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          "gene_symbol": "LTA4H",
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          "hgvs_c": "c.1308-1063A>T",
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          "strand": false,
          "consequences": [
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          ],
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          "exon_count": 18,
          "intron_rank": 14,
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          "gene_symbol": "LTA4H",
          "gene_hgnc_id": 6710,
          "hgvs_c": "c.1308-1063A>T",
          "hgvs_p": null,
          "transcript": "ENST00000413268.6",
          "protein_id": "ENSP00000395051.2",
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        },
        {
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 20,
          "intron_rank": 15,
          "intron_rank_end": null,
          "gene_symbol": "LTA4H",
          "gene_hgnc_id": 6710,
          "hgvs_c": "c.744-1063A>T",
          "hgvs_p": null,
          "transcript": "NM_001414266.1",
          "protein_id": "NP_001401195.1",
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        {
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          ],
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          "intron_rank": 1,
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          "strand": false,
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          ],
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          "intron_rank": 5,
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          "gene_symbol": "LTA4H",
          "gene_hgnc_id": 6710,
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        },
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          "strand": false,
          "consequences": [
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          ],
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          "exon_count": 18,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "LTA4H",
          "gene_hgnc_id": 6710,
          "hgvs_c": "n.*920-1063A>T",
          "hgvs_p": null,
          "transcript": "ENST00000548852.5",
          "protein_id": "ENSP00000449340.1",
          "transcript_support_level": 2,
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          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000257878",
          "gene_hgnc_id": null,
          "hgvs_c": "n.451+141T>A",
          "hgvs_p": null,
          "transcript": "ENST00000551849.2",
          "protein_id": null,
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      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
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      "custom_annotations": null
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  "message": null
}