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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: 1-21003621-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=21003621&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "1",
      "pos": 21003621,
      "ref": "G",
      "alt": "A",
      "effect": "intron_variant",
      "transcript": "ENST00000602326.6",
      "consequences": [
        {
          "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": 37,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "EIF4G3",
          "gene_hgnc_id": 3298,
          "hgvs_c": "c.-66-813C>T",
          "hgvs_p": null,
          "transcript": "NM_001391906.1",
          "protein_id": "NP_001378835.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1641,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 4926,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6397,
          "mane_select": "ENST00000602326.6",
          "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": 37,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "EIF4G3",
          "gene_hgnc_id": 3298,
          "hgvs_c": "c.-66-813C>T",
          "hgvs_p": null,
          "transcript": "ENST00000602326.6",
          "protein_id": "ENSP00000473510.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1641,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 4926,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6397,
          "mane_select": "NM_001391906.1",
          "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": 35,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "EIF4G3",
          "gene_hgnc_id": 3298,
          "hgvs_c": "c.-66-813C>T",
          "hgvs_p": null,
          "transcript": "ENST00000400422.6",
          "protein_id": "ENSP00000383274.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1621,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 4866,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5762,
          "mane_select": null,
          "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": 15,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "EIF4G3",
          "gene_hgnc_id": 3298,
          "hgvs_c": "c.-66-813C>T",
          "hgvs_p": null,
          "transcript": "ENST00000356916.7",
          "protein_id": "ENSP00000349386.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 515,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1548,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2179,
          "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": 1,
          "exon_rank_end": null,
          "exon_count": 1,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS15AP6",
          "gene_hgnc_id": 35657,
          "hgvs_c": "n.314C>T",
          "hgvs_p": null,
          "transcript": "ENST00000420703.1",
          "protein_id": null,
          "transcript_support_level": 6,
          "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": 385,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": null,
          "protein_coding": null,
          "strand": true,
          "consequences": [
            "intragenic_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPS15AP6",
          "gene_hgnc_id": 35657,
          "hgvs_c": "n.21003621G>A",
          "hgvs_p": null,
          "transcript": null,
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "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": 33,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "EIF4G3",
          "gene_hgnc_id": 3298,
          "hgvs_c": "c.868-813C>T",
          "hgvs_p": null,
          "transcript": "ENST00000693470.1",
          "protein_id": "ENSP00000509295.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1895,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5688,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5688,
          "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": 34,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "EIF4G3",
          "gene_hgnc_id": 3298,
          "hgvs_c": "c.505-813C>T",
          "hgvs_p": null,
          "transcript": "ENST00000634879.2",
          "protein_id": "ENSP00000489051.2",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1774,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5325,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5325,
          "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": 33,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "EIF4G3",
          "gene_hgnc_id": 3298,
          "hgvs_c": "c.424-813C>T",
          "hgvs_p": null,
          "transcript": "ENST00000685872.1",
          "protein_id": "ENSP00000509442.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1747,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5244,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6528,
          "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": 37,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "EIF4G3",
          "gene_hgnc_id": 3298,
          "hgvs_c": "c.-66-813C>T",
          "hgvs_p": null,
          "transcript": "NM_001391907.1",
          "protein_id": "NP_001378836.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1671,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5016,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6487,
          "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": 36,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "EIF4G3",
          "gene_hgnc_id": 3298,
          "hgvs_c": "c.-66-813C>T",
          "hgvs_p": null,
          "transcript": "ENST00000684485.1",
          "protein_id": "ENSP00000507662.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1640,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 4923,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7832,
          "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": 36,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "EIF4G3",
          "gene_hgnc_id": 3298,
          "hgvs_c": "c.-66-813C>T",
          "hgvs_p": null,
          "transcript": "NM_001438678.1",
          "protein_id": "NP_001425607.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1634,
          "cds_start": -4,
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          "cds_length": 4905,
          "cdna_start": null,
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          "cdna_length": 6253,
          "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": 35,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "EIF4G3",
          "gene_hgnc_id": 3298,
          "hgvs_c": "c.-66-813C>T",
          "hgvs_p": null,
          "transcript": "NM_001438679.1",
          "protein_id": "NP_001425608.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 1634,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 4905,
          "cdna_start": null,
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          "cdna_length": 6070,
          "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": 36,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "EIF4G3",
          "gene_hgnc_id": 3298,
          "hgvs_c": "c.-66-813C>T",
          "hgvs_p": null,
          "transcript": "NM_001391905.1",
          "protein_id": "NP_001378834.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1633,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 4902,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6250,
          "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": 35,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "EIF4G3",
          "gene_hgnc_id": 3298,
          "hgvs_c": "c.-66-813C>T",
          "hgvs_p": null,
          "transcript": "ENST00000688741.1",
          "protein_id": "ENSP00000509547.1",
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          "cds_start": -4,
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          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 35,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "EIF4G3",
          "gene_hgnc_id": 3298,
          "hgvs_c": "c.-66-813C>T",
          "hgvs_p": null,
          "transcript": "NM_001391902.1",
          "protein_id": "NP_001378831.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1622,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 4869,
          "cdna_start": null,
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          "cdna_length": 6340,
          "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": 34,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "EIF4G3",
          "gene_hgnc_id": 3298,
          "hgvs_c": "c.-66-813C>T",
          "hgvs_p": null,
          "transcript": "NM_001391903.1",
          "protein_id": "NP_001378832.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1622,
          "cds_start": -4,
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          "cds_length": 4869,
          "cdna_start": null,
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          "cdna_length": 6156,
          "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": 35,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "EIF4G3",
          "gene_hgnc_id": 3298,
          "hgvs_c": "c.-66-813C>T",
          "hgvs_p": null,
          "transcript": "NM_001391904.1",
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          "biotype": null,
          "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": 35,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "EIF4G3",
          "gene_hgnc_id": 3298,
          "hgvs_c": "c.-66-813C>T",
          "hgvs_p": null,
          "transcript": "NM_001198801.3",
          "protein_id": "NP_001185730.1",
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          "cdna_length": 6337,
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          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 35,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "EIF4G3",
          "gene_hgnc_id": 3298,
          "hgvs_c": "c.-66-813C>T",
          "hgvs_p": null,
          "transcript": "NM_001391901.1",
          "protein_id": "NP_001378830.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 1592,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 4779,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6250,
          "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": 35,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "EIF4G3",
          "gene_hgnc_id": 3298,
          "hgvs_c": "c.-66-813C>T",
          "hgvs_p": null,
          "transcript": "NM_001198802.3",
          "protein_id": "NP_001185731.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
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      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}