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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: 19-54636725-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=54636725&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "19",
      "pos": 54636725,
      "ref": "G",
      "alt": "A",
      "effect": "splice_region_variant,intron_variant",
      "transcript": "NM_001081637.3",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "LILRB1",
          "gene_hgnc_id": 6605,
          "hgvs_c": "c.1813-7G>A",
          "hgvs_p": null,
          "transcript": "NM_001081637.3",
          "protein_id": "NP_001075106.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 652,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1959,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000324602.12",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001081637.3"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "LILRB1",
          "gene_hgnc_id": 6605,
          "hgvs_c": "c.1813-7G>A",
          "hgvs_p": null,
          "transcript": "ENST00000324602.12",
          "protein_id": "ENSP00000315997.7",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 652,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1959,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_001081637.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000324602.12"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": 13,
          "intron_rank_end": null,
          "gene_symbol": "LILRB1",
          "gene_hgnc_id": 6605,
          "hgvs_c": "c.1813-7G>A",
          "hgvs_p": null,
          "transcript": "ENST00000396315.5",
          "protein_id": "ENSP00000379608.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 652,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1959,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000396315.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "LILRB1",
          "gene_hgnc_id": 6605,
          "hgvs_c": "c.1810-7G>A",
          "hgvs_p": null,
          "transcript": "ENST00000396327.7",
          "protein_id": "ENSP00000379618.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 651,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1956,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000396327.7"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "LILRB1",
          "gene_hgnc_id": 6605,
          "hgvs_c": "c.1810-7G>A",
          "hgvs_p": null,
          "transcript": "ENST00000396332.8",
          "protein_id": "ENSP00000379623.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 651,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1956,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000396332.8"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": 15,
          "intron_rank_end": null,
          "gene_symbol": "LILRB1",
          "gene_hgnc_id": 6605,
          "hgvs_c": "c.1807-7G>A",
          "hgvs_p": null,
          "transcript": "ENST00000396331.5",
          "protein_id": "ENSP00000379622.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 650,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1953,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000396331.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": 12,
          "intron_rank_end": null,
          "gene_symbol": "LILRB1",
          "gene_hgnc_id": 6605,
          "hgvs_c": "c.1759-7G>A",
          "hgvs_p": null,
          "transcript": "ENST00000396317.5",
          "protein_id": "ENSP00000379610.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 634,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1905,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000396317.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "LILRB1",
          "gene_hgnc_id": 6605,
          "hgvs_c": "c.1960-7G>A",
          "hgvs_p": null,
          "transcript": "ENST00000427581.6",
          "protein_id": "ENSP00000395004.2",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 701,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2106,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000427581.6"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": 15,
          "intron_rank_end": null,
          "gene_symbol": "LILRB1",
          "gene_hgnc_id": 6605,
          "hgvs_c": "c.1843-7G>A",
          "hgvs_p": null,
          "transcript": "ENST00000955136.1",
          "protein_id": "ENSP00000625195.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 662,
          "cds_start": null,
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          "cds_length": 1989,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000955136.1"
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 15,
          "intron_rank": 14,
          "intron_rank_end": null,
          "gene_symbol": "LILRB1",
          "gene_hgnc_id": 6605,
          "hgvs_c": "c.1840-7G>A",
          "hgvs_p": null,
          "transcript": "ENST00000890799.1",
          "protein_id": "ENSP00000560858.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_start": null,
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          "cdna_start": null,
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        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 15,
          "intron_rank": 14,
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          "gene_symbol": "LILRB1",
          "gene_hgnc_id": 6605,
          "hgvs_c": "c.1840-7G>A",
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          "transcript": "ENST00000955144.1",
          "protein_id": "ENSP00000625203.1",
          "transcript_support_level": null,
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          "cds_start": null,
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          "intron_rank": 15,
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          "gene_symbol": "LILRB1",
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          "cds_start": null,
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        {
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            "intron_variant"
          ],
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          "gene_symbol": "LILRB1",
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          "transcript": "NM_001388358.1",
          "protein_id": "NP_001375287.1",
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        },
        {
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            "intron_variant"
          ],
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          "gene_symbol": "LILRB1",
          "gene_hgnc_id": 6605,
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          "transcript": "NM_001081638.4",
          "protein_id": "NP_001075107.2",
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          "gene_symbol": "LILRB1",
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          "transcript": "NM_001081639.4",
          "protein_id": "NP_001075108.2",
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        {
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            "intron_variant"
          ],
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          "intron_rank": 15,
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          "gene_symbol": "LILRB1",
          "gene_hgnc_id": 6605,
          "hgvs_c": "c.1810-7G>A",
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          "transcript": "NM_001388355.1",
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        {
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          "protein_coding": true,
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          "consequences": [
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            "intron_variant"
          ],
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          "intron_rank": 15,
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          "gene_symbol": "LILRB1",
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        {
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          "gene_symbol": "LILRB1",
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        {
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          "gene_symbol": "LILRB1",
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          "transcript": "ENST00000890795.1",
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          "biotype": "protein_coding",
          "feature": "ENST00000890795.1"
        },
        {
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          "protein_coding": true,
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          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 16,
          "intron_rank": 15,
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          "gene_symbol": "LILRB1",
          "gene_hgnc_id": 6605,
          "hgvs_c": "c.1810-7G>A",
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          "transcript": "ENST00000890796.1",
          "protein_id": "ENSP00000560855.1",
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      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
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      "custom_annotations": null
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  "message": null
}