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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: 2-209684454-C-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=209684454&ref=C&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 209684454,
      "ref": "C",
      "alt": "G",
      "effect": "intron_variant",
      "transcript": "ENST00000682079.1",
      "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": 16,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "MAP2",
          "gene_hgnc_id": 6839,
          "hgvs_c": "c.454+3627C>G",
          "hgvs_p": null,
          "transcript": "NM_001375505.1",
          "protein_id": "NP_001362434.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1827,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5484,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 9650,
          "mane_select": "ENST00000682079.1",
          "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": 16,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "MAP2",
          "gene_hgnc_id": 6839,
          "hgvs_c": "c.454+3627C>G",
          "hgvs_p": null,
          "transcript": "ENST00000682079.1",
          "protein_id": "ENSP00000507035.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1827,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5484,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 9650,
          "mane_select": "NM_001375505.1",
          "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": 12,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "MAP2",
          "gene_hgnc_id": 6839,
          "hgvs_c": "c.454+3627C>G",
          "hgvs_p": null,
          "transcript": "ENST00000447185.5",
          "protein_id": "ENSP00000392164.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1823,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5472,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5472,
          "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": 15,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "MAP2",
          "gene_hgnc_id": 6839,
          "hgvs_c": "c.454+3627C>G",
          "hgvs_p": null,
          "transcript": "ENST00000199940.10",
          "protein_id": "ENSP00000199940.6",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 559,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1680,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2241,
          "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": 12,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "MAP2",
          "gene_hgnc_id": 6839,
          "hgvs_c": "c.454+3627C>G",
          "hgvs_p": null,
          "transcript": "ENST00000361559.8",
          "protein_id": "ENSP00000355290.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 471,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1416,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2038,
          "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": 11,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "MAP2",
          "gene_hgnc_id": 6839,
          "hgvs_c": "c.454+3627C>G",
          "hgvs_p": null,
          "transcript": "ENST00000392194.5",
          "protein_id": "ENSP00000376032.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 471,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1416,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5303,
          "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": 17,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "MAP2",
          "gene_hgnc_id": 6839,
          "hgvs_c": "c.455-3265C>G",
          "hgvs_p": null,
          "transcript": "ENST00000673860.1",
          "protein_id": "ENSP00000501117.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1990,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5973,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 10012,
          "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": 18,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "MAP2",
          "gene_hgnc_id": 6839,
          "hgvs_c": "c.454+3627C>G",
          "hgvs_p": null,
          "transcript": "NM_001375504.1",
          "protein_id": "NP_001362433.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1915,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5748,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 9914,
          "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": 17,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "MAP2",
          "gene_hgnc_id": 6839,
          "hgvs_c": "c.454+3627C>G",
          "hgvs_p": null,
          "transcript": "NM_001375501.1",
          "protein_id": "NP_001362430.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1909,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5730,
          "cdna_start": null,
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          "cdna_length": 9896,
          "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": 16,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "MAP2",
          "gene_hgnc_id": 6839,
          "hgvs_c": "c.454+3627C>G",
          "hgvs_p": null,
          "transcript": "NM_001375537.1",
          "protein_id": "NP_001362466.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1909,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5730,
          "cdna_start": null,
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          "cdna_length": 9765,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          "exon_count": 16,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "MAP2",
          "gene_hgnc_id": 6839,
          "hgvs_c": "c.454+3627C>G",
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          "transcript": "NM_001375531.1",
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          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 1908,
          "cds_start": -4,
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          "cds_length": 5727,
          "cdna_start": null,
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          "cdna_length": 9762,
          "mane_select": null,
          "mane_plus": null,
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          "feature": null
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        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
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          "exon_count": 16,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "MAP2",
          "gene_hgnc_id": 6839,
          "hgvs_c": "c.454+3627C>G",
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          "transcript": "NM_001375539.1",
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          "cds_start": -4,
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          "gene_symbol": "MAP2",
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          "hgvs_c": "c.454+3627C>G",
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        {
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          "gene_symbol": "MAP2",
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          "hgvs_c": "c.454+3627C>G",
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        {
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          "gene_symbol": "MAP2",
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          "gene_symbol": "MAP2",
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          "intron_rank": 7,
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        {
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          ],
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          "intron_rank": 6,
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          "gene_symbol": "MAP2",
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          "gene_symbol": "MAP2",
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          "gene_symbol": "MAP2",
          "gene_hgnc_id": 6839,
          "hgvs_c": "c.454+3627C>G",
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