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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: 21-29157697-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=21&pos=29157697&ref=A&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "21",
      "pos": 29157697,
      "ref": "A",
      "alt": "G",
      "effect": "intron_variant",
      "transcript": "ENST00000399928.6",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "MAP3K7CL",
          "gene_hgnc_id": 16457,
          "hgvs_c": "c.133-2244A>G",
          "hgvs_p": null,
          "transcript": "NM_001286620.2",
          "protein_id": "NP_001273549.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 142,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 429,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1743,
          "mane_select": "ENST00000399928.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "MAP3K7CL",
          "gene_hgnc_id": 16457,
          "hgvs_c": "c.133-2244A>G",
          "hgvs_p": null,
          "transcript": "ENST00000399928.6",
          "protein_id": "ENSP00000382812.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 142,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 429,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1743,
          "mane_select": "NM_001286620.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "MAP3K7CL",
          "gene_hgnc_id": 16457,
          "hgvs_c": "c.433-2244A>G",
          "hgvs_p": null,
          "transcript": "ENST00000341618.8",
          "protein_id": "ENSP00000343212.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 242,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 729,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1855,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "MAP3K7CL",
          "gene_hgnc_id": 16457,
          "hgvs_c": "c.433-2244A>G",
          "hgvs_p": null,
          "transcript": "ENST00000399947.6",
          "protein_id": "ENSP00000382828.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 242,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 729,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2003,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "MAP3K7CL",
          "gene_hgnc_id": 16457,
          "hgvs_c": "c.133-2244A>G",
          "hgvs_p": null,
          "transcript": "ENST00000399925.5",
          "protein_id": "ENSP00000382809.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 142,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 429,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 692,
          "mane_select": null,
          "mane_plus": null,
          "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": 4,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "MAP3K7CL",
          "gene_hgnc_id": 16457,
          "hgvs_c": "n.222-2244A>G",
          "hgvs_p": null,
          "transcript": "ENST00000460883.5",
          "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": 655,
          "mane_select": null,
          "mane_plus": null,
          "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": 4,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "MAP3K7CL",
          "gene_hgnc_id": 16457,
          "hgvs_c": "n.212-2244A>G",
          "hgvs_p": null,
          "transcript": "ENST00000470800.1",
          "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": 835,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "MAP3K7CL",
          "gene_hgnc_id": 16457,
          "hgvs_c": "c.433-2244A>G",
          "hgvs_p": null,
          "transcript": "NM_001286634.2",
          "protein_id": "NP_001273563.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 242,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 729,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2372,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "MAP3K7CL",
          "gene_hgnc_id": 16457,
          "hgvs_c": "c.433-2244A>G",
          "hgvs_p": null,
          "transcript": "NM_001371369.1",
          "protein_id": "NP_001358298.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 242,
          "cds_start": -4,
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          "cds_length": 729,
          "cdna_start": null,
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          "cdna_length": 2529,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "MAP3K7CL",
          "gene_hgnc_id": 16457,
          "hgvs_c": "c.433-2244A>G",
          "hgvs_p": null,
          "transcript": "NM_020152.4",
          "protein_id": "NP_064537.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 242,
          "cds_start": -4,
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          "cds_length": 729,
          "cdna_start": null,
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          "cdna_length": 2601,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
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          "strand": true,
          "consequences": [
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          "exon_count": 6,
          "intron_rank": 4,
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          "gene_symbol": "MAP3K7CL",
          "gene_hgnc_id": 16457,
          "hgvs_c": "c.316-2244A>G",
          "hgvs_p": null,
          "transcript": "NM_001371370.1",
          "protein_id": "NP_001358299.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 203,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 1816,
          "mane_select": null,
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          "biotype": null,
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
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          "consequences": [
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          ],
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          "exon_count": 5,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "MAP3K7CL",
          "gene_hgnc_id": 16457,
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          "protein_id": "NP_001358300.1",
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        {
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          "intron_rank": 8,
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          "gene_symbol": "MAP3K7CL",
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          "hgvs_c": "c.133-2244A>G",
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          "gene_symbol": "MAP3K7CL",
          "gene_hgnc_id": 16457,
          "hgvs_c": "c.133-2244A>G",
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          "transcript": "NM_001286618.2",
          "protein_id": "NP_001273547.1",
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        {
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          "gene_symbol": "MAP3K7CL",
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          "hgvs_c": "c.133-2244A>G",
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          "transcript": "NM_001371372.1",
          "protein_id": "NP_001358301.1",
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        {
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          "gene_symbol": "MAP3K7CL",
          "gene_hgnc_id": 16457,
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          "transcript": "NM_001371373.1",
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        {
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          "intron_rank": 10,
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          "gene_hgnc_id": 16457,
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        {
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          "gene_symbol": "MAP3K7CL",
          "gene_hgnc_id": 16457,
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          "transcript": "ENST00000399926.5",
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          "feature": null
        },
        {
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          "consequences": [
            "intron_variant"
          ],
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          "exon_count": 9,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "MAP3K7CL",
          "gene_hgnc_id": 16457,
          "hgvs_c": "c.133-2244A>G",
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          "transcript": "ENST00000399934.5",
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      "clinvar_classification": "",
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      "custom_annotations": null
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  "message": null
}