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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: 9-34656818-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=9&pos=34656818&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "9",
      "pos": 34656818,
      "ref": "C",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "NM_001142784.3",
      "consequences": [
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IL11RA",
          "gene_hgnc_id": 5967,
          "hgvs_c": "c.241C>T",
          "hgvs_p": "p.Leu81Leu",
          "transcript": "NM_001142784.3",
          "protein_id": "NP_001136256.1",
          "transcript_support_level": null,
          "aa_start": 81,
          "aa_end": null,
          "aa_length": 422,
          "cds_start": 241,
          "cds_end": null,
          "cds_length": 1269,
          "cdna_start": 290,
          "cdna_end": null,
          "cdna_length": 1722,
          "mane_select": "ENST00000441545.7",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001142784.3"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IL11RA",
          "gene_hgnc_id": 5967,
          "hgvs_c": "c.241C>T",
          "hgvs_p": "p.Leu81Leu",
          "transcript": "ENST00000441545.7",
          "protein_id": "ENSP00000394391.3",
          "transcript_support_level": 5,
          "aa_start": 81,
          "aa_end": null,
          "aa_length": 422,
          "cds_start": 241,
          "cds_end": null,
          "cds_length": 1269,
          "cdna_start": 290,
          "cdna_end": null,
          "cdna_length": 1722,
          "mane_select": "NM_001142784.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000441545.7"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IL11RA",
          "gene_hgnc_id": 5967,
          "hgvs_c": "c.241C>T",
          "hgvs_p": "p.Leu81Leu",
          "transcript": "ENST00000318041.13",
          "protein_id": "ENSP00000326500.8",
          "transcript_support_level": 1,
          "aa_start": 81,
          "aa_end": null,
          "aa_length": 422,
          "cds_start": 241,
          "cds_end": null,
          "cds_length": 1269,
          "cdna_start": 306,
          "cdna_end": null,
          "cdna_length": 1728,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000318041.13"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IL11RA",
          "gene_hgnc_id": 5967,
          "hgvs_c": "c.241C>T",
          "hgvs_p": "p.Leu81Leu",
          "transcript": "ENST00000602473.5",
          "protein_id": "ENSP00000473647.1",
          "transcript_support_level": 1,
          "aa_start": 81,
          "aa_end": null,
          "aa_length": 390,
          "cds_start": 241,
          "cds_end": null,
          "cds_length": 1173,
          "cdna_start": 241,
          "cdna_end": null,
          "cdna_length": 1388,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000602473.5"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000258728",
          "gene_hgnc_id": null,
          "hgvs_c": "c.673C>T",
          "hgvs_p": "p.Leu225Leu",
          "transcript": "ENST00000556278.1",
          "protein_id": "ENSP00000451792.1",
          "transcript_support_level": 5,
          "aa_start": 225,
          "aa_end": null,
          "aa_length": 279,
          "cds_start": 673,
          "cds_end": null,
          "cds_length": 842,
          "cdna_start": 733,
          "cdna_end": null,
          "cdna_length": 902,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000556278.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IL11RA",
          "gene_hgnc_id": 5967,
          "hgvs_c": "c.406C>T",
          "hgvs_p": "p.Leu136Leu",
          "transcript": "ENST00000957059.1",
          "protein_id": "ENSP00000627118.1",
          "transcript_support_level": null,
          "aa_start": 136,
          "aa_end": null,
          "aa_length": 477,
          "cds_start": 406,
          "cds_end": null,
          "cds_length": 1434,
          "cdna_start": 1793,
          "cdna_end": null,
          "cdna_length": 3209,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000957059.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IL11RA",
          "gene_hgnc_id": 5967,
          "hgvs_c": "c.253C>T",
          "hgvs_p": "p.Leu85Leu",
          "transcript": "ENST00000957054.1",
          "protein_id": "ENSP00000627113.1",
          "transcript_support_level": null,
          "aa_start": 85,
          "aa_end": null,
          "aa_length": 430,
          "cds_start": 253,
          "cds_end": null,
          "cds_length": 1293,
          "cdna_start": 288,
          "cdna_end": null,
          "cdna_length": 1716,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000957054.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IL11RA",
          "gene_hgnc_id": 5967,
          "hgvs_c": "c.256C>T",
          "hgvs_p": "p.Leu86Leu",
          "transcript": "ENST00000902566.1",
          "protein_id": "ENSP00000572625.1",
          "transcript_support_level": null,
          "aa_start": 86,
          "aa_end": null,
          "aa_length": 427,
          "cds_start": 256,
          "cds_end": null,
          "cds_length": 1284,
          "cdna_start": 286,
          "cdna_end": null,
          "cdna_length": 1710,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000902566.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IL11RA",
          "gene_hgnc_id": 5967,
          "hgvs_c": "c.256C>T",
          "hgvs_p": "p.Leu86Leu",
          "transcript": "ENST00000957061.1",
          "protein_id": "ENSP00000627120.1",
          "transcript_support_level": null,
          "aa_start": 86,
          "aa_end": null,
          "aa_length": 427,
          "cds_start": 256,
          "cds_end": null,
          "cds_length": 1284,
          "cdna_start": 382,
          "cdna_end": null,
          "cdna_length": 1793,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000957061.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IL11RA",
          "gene_hgnc_id": 5967,
          "hgvs_c": "c.241C>T",
          "hgvs_p": "p.Leu81Leu",
          "transcript": "ENST00000555003.6",
          "protein_id": "ENSP00000450565.2",
          "transcript_support_level": 2,
          "aa_start": 81,
          "aa_end": null,
          "aa_length": 426,
          "cds_start": 241,
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          "cds_length": 1281,
          "cdna_start": 290,
          "cdna_end": null,
          "cdna_length": 1734,
          "mane_select": null,
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
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          "gene_symbol": "IL11RA",
          "gene_hgnc_id": 5967,
          "hgvs_c": "c.241C>T",
          "hgvs_p": "p.Leu81Leu",
          "transcript": "ENST00000902558.1",
          "protein_id": "ENSP00000572617.1",
          "transcript_support_level": null,
          "aa_start": 81,
          "aa_end": null,
          "aa_length": 426,
          "cds_start": 241,
          "cds_end": null,
          "cds_length": 1281,
          "cdna_start": 649,
          "cdna_end": null,
          "cdna_length": 2071,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000902558.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 4,
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          "exon_count": 13,
          "intron_rank": null,
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          "gene_symbol": "IL11RA",
          "gene_hgnc_id": 5967,
          "hgvs_c": "c.253C>T",
          "hgvs_p": "p.Leu85Leu",
          "transcript": "ENST00000902560.1",
          "protein_id": "ENSP00000572619.1",
          "transcript_support_level": null,
          "aa_start": 85,
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          "aa_length": 426,
          "cds_start": 253,
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          "cds_length": 1281,
          "cdna_start": 308,
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          "cdna_length": 1740,
          "mane_select": null,
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
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          "intron_rank": null,
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          "gene_symbol": "IL11RA",
          "gene_hgnc_id": 5967,
          "hgvs_c": "c.241C>T",
          "hgvs_p": "p.Leu81Leu",
          "transcript": "ENST00000902561.1",
          "protein_id": "ENSP00000572620.1",
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          "cds_start": 241,
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          "cdna_start": 380,
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          "cdna_length": 1824,
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
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          "gene_symbol": "IL11RA",
          "gene_hgnc_id": 5967,
          "hgvs_c": "c.253C>T",
          "hgvs_p": "p.Leu85Leu",
          "transcript": "ENST00000902569.1",
          "protein_id": "ENSP00000572628.1",
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          "cds_start": 253,
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        {
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          ],
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          "intron_rank": null,
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          "gene_symbol": "IL11RA",
          "gene_hgnc_id": 5967,
          "hgvs_c": "c.241C>T",
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          "transcript": "ENST00000902571.1",
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          "cdna_start": 348,
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          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000902571.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          "exon_rank": 4,
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          "gene_symbol": "IL11RA",
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          "hgvs_c": "c.241C>T",
          "hgvs_p": "p.Leu81Leu",
          "transcript": "ENST00000957058.1",
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        },
        {
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          "consequences": [
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          ],
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          "exon_count": 12,
          "intron_rank": null,
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          "gene_symbol": "IL11RA",
          "gene_hgnc_id": 5967,
          "hgvs_c": "c.241C>T",
          "hgvs_p": "p.Leu81Leu",
          "transcript": "ENST00000957065.1",
          "protein_id": "ENSP00000627124.1",
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        {
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        {
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          "gene_symbol": "IL11RA",
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          "transcript": "ENST00000957053.1",
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          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000957053.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IL11RA",
          "gene_hgnc_id": 5967,
          "hgvs_c": "c.241C>T",
          "hgvs_p": "p.Leu81Leu",
          "transcript": "ENST00000555981.6",
          "protein_id": "ENSP00000450640.2",
          "transcript_support_level": 2,
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          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000557298.5"
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      ],
      "gene_symbol": "IL11RA",
      "gene_hgnc_id": 5967,
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      "computational_score_selected": -0.5400000214576721,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
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      "alphamissense_score": null,
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      "bayesdelnoaf_score": -0.54,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.573,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
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      "mitotip_score": null,
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      "acmg_score": -11,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Moderate,BP7,BS1",
      "acmg_by_gene": [
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          "pathogenic_score": 0,
          "criteria": [
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            "BP6_Moderate",
            "BP7",
            "BS1"
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          "verdict": "Benign",
          "transcript": "NM_001142784.3",
          "gene_symbol": "IL11RA",
          "hgnc_id": 5967,
          "effects": [
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          "inheritance_mode": "AR",
          "hgvs_c": "c.241C>T",
          "hgvs_p": "p.Leu81Leu"
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        {
          "score": -7,
          "benign_score": 7,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Moderate",
            "BP7"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000556278.1",
          "gene_symbol": "ENSG00000258728",
          "hgnc_id": null,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "c.673C>T",
          "hgvs_p": "p.Leu225Leu"
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      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "B:1",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Benign",
      "custom_annotations": null
    }
  ],
  "message": null
}
For research and educational, non-commercial use only. Not for clinical or diagnostic use. GeneBe does not provide medical advice. Data use for AI modeling is prohibited: if used, the cost is $0.001 per byte of downloaded uncompressed data.