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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: 1-53266643-G-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=53266643&ref=G&alt=T&genome=hg38&allGenes=true"API Response
json
{
  "variants": [
    {
      "chr": "1",
      "pos": 53266643,
      "ref": "G",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "ENST00000306052.12",
      "consequences": [
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LRP8",
          "gene_hgnc_id": 6700,
          "hgvs_c": "c.1257C>A",
          "hgvs_p": "p.Gly419Gly",
          "transcript": "NM_004631.5",
          "protein_id": "NP_004622.2",
          "transcript_support_level": null,
          "aa_start": 419,
          "aa_end": null,
          "aa_length": 963,
          "cds_start": 1257,
          "cds_end": null,
          "cds_length": 2892,
          "cdna_start": 1415,
          "cdna_end": null,
          "cdna_length": 7704,
          "mane_select": "ENST00000306052.12",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LRP8",
          "gene_hgnc_id": 6700,
          "hgvs_c": "c.1257C>A",
          "hgvs_p": "p.Gly419Gly",
          "transcript": "ENST00000306052.12",
          "protein_id": "ENSP00000303634.6",
          "transcript_support_level": 1,
          "aa_start": 419,
          "aa_end": null,
          "aa_length": 963,
          "cds_start": 1257,
          "cds_end": null,
          "cds_length": 2892,
          "cdna_start": 1415,
          "cdna_end": null,
          "cdna_length": 7704,
          "mane_select": "NM_004631.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LRP8",
          "gene_hgnc_id": 6700,
          "hgvs_c": "c.1257C>A",
          "hgvs_p": "p.Gly419Gly",
          "transcript": "ENST00000371454.6",
          "protein_id": "ENSP00000360509.2",
          "transcript_support_level": 1,
          "aa_start": 419,
          "aa_end": null,
          "aa_length": 904,
          "cds_start": 1257,
          "cds_end": null,
          "cds_length": 2715,
          "cdna_start": 1399,
          "cdna_end": null,
          "cdna_length": 3322,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LRP8",
          "gene_hgnc_id": 6700,
          "hgvs_c": "c.747C>A",
          "hgvs_p": "p.Gly249Gly",
          "transcript": "ENST00000347547.7",
          "protein_id": "ENSP00000334522.2",
          "transcript_support_level": 1,
          "aa_start": 249,
          "aa_end": null,
          "aa_length": 793,
          "cds_start": 747,
          "cds_end": null,
          "cds_length": 2382,
          "cdna_start": 757,
          "cdna_end": null,
          "cdna_length": 2392,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LRP8",
          "gene_hgnc_id": 6700,
          "hgvs_c": "c.870C>A",
          "hgvs_p": "p.Gly290Gly",
          "transcript": "ENST00000354412.7",
          "protein_id": "ENSP00000346391.3",
          "transcript_support_level": 1,
          "aa_start": 290,
          "aa_end": null,
          "aa_length": 700,
          "cds_start": 870,
          "cds_end": null,
          "cds_length": 2103,
          "cdna_start": 870,
          "cdna_end": null,
          "cdna_length": 2553,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LRP8",
          "gene_hgnc_id": 6700,
          "hgvs_c": "c.1257C>A",
          "hgvs_p": "p.Gly419Gly",
          "transcript": "ENST00000667377.1",
          "protein_id": "ENSP00000499405.1",
          "transcript_support_level": null,
          "aa_start": 419,
          "aa_end": null,
          "aa_length": 926,
          "cds_start": 1257,
          "cds_end": null,
          "cds_length": 2781,
          "cdna_start": 1402,
          "cdna_end": null,
          "cdna_length": 3258,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LRP8",
          "gene_hgnc_id": 6700,
          "hgvs_c": "c.1257C>A",
          "hgvs_p": "p.Gly419Gly",
          "transcript": "NM_001018054.3",
          "protein_id": "NP_001018064.1",
          "transcript_support_level": null,
          "aa_start": 419,
          "aa_end": null,
          "aa_length": 904,
          "cds_start": 1257,
          "cds_end": null,
          "cds_length": 2715,
          "cdna_start": 1415,
          "cdna_end": null,
          "cdna_length": 7527,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LRP8",
          "gene_hgnc_id": 6700,
          "hgvs_c": "c.1257C>A",
          "hgvs_p": "p.Gly419Gly",
          "transcript": "ENST00000659993.1",
          "protein_id": "ENSP00000499697.1",
          "transcript_support_level": null,
          "aa_start": 419,
          "aa_end": null,
          "aa_length": 888,
          "cds_start": 1257,
          "cds_end": null,
          "cds_length": 2667,
          "cdna_start": 1369,
          "cdna_end": null,
          "cdna_length": 3477,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LRP8",
          "gene_hgnc_id": 6700,
          "hgvs_c": "c.1257C>A",
          "hgvs_p": "p.Gly419Gly",
          "transcript": "ENST00000668448.1",
          "protein_id": "ENSP00000499273.1",
          "transcript_support_level": null,
          "aa_start": 419,
          "aa_end": null,
          "aa_length": 888,
          "cds_start": 1257,
          "cds_end": null,
          "cds_length": 2667,
          "cdna_start": 1441,
          "cdna_end": null,
          "cdna_length": 4324,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LRP8",
          "gene_hgnc_id": 6700,
          "hgvs_c": "c.891C>A",
          "hgvs_p": "p.Gly297Gly",
          "transcript": "ENST00000465675.6",
          "protein_id": "ENSP00000437009.2",
          "transcript_support_level": 2,
          "aa_start": 297,
          "aa_end": null,
          "aa_length": 841,
          "cds_start": 891,
          "cds_end": null,
          "cds_length": 2526,
          "cdna_start": 891,
          "cdna_end": null,
          "cdna_length": 2992,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LRP8",
          "gene_hgnc_id": 6700,
          "hgvs_c": "c.870C>A",
          "hgvs_p": "p.Gly290Gly",
          "transcript": "ENST00000662198.1",
          "protein_id": "ENSP00000499355.1",
          "transcript_support_level": null,
          "aa_start": 290,
          "aa_end": null,
          "aa_length": 834,
          "cds_start": 870,
          "cds_end": null,
          "cds_length": 2505,
          "cdna_start": 1427,
          "cdna_end": null,
          "cdna_length": 4534,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LRP8",
          "gene_hgnc_id": 6700,
          "hgvs_c": "c.792C>A",
          "hgvs_p": "p.Gly264Gly",
          "transcript": "ENST00000653217.1",
          "protein_id": "ENSP00000499777.1",
          "transcript_support_level": null,
          "aa_start": 264,
          "aa_end": null,
          "aa_length": 808,
          "cds_start": 792,
          "cds_end": null,
          "cds_length": 2427,
          "cdna_start": 792,
          "cdna_end": null,
          "cdna_length": 3854,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LRP8",
          "gene_hgnc_id": 6700,
          "hgvs_c": "c.747C>A",
          "hgvs_p": "p.Gly249Gly",
          "transcript": "NM_033300.4",
          "protein_id": "NP_150643.2",
          "transcript_support_level": null,
          "aa_start": 249,
          "aa_end": null,
          "aa_length": 793,
          "cds_start": 747,
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          "cdna_start": 905,
          "cdna_end": null,
          "cdna_length": 7194,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LRP8",
          "gene_hgnc_id": 6700,
          "hgvs_c": "c.744C>A",
          "hgvs_p": "p.Gly248Gly",
          "transcript": "ENST00000657895.1",
          "protein_id": "ENSP00000499764.1",
          "transcript_support_level": null,
          "aa_start": 248,
          "aa_end": null,
          "aa_length": 790,
          "cds_start": 744,
          "cds_end": null,
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          "cdna_start": 862,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
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          "gene_symbol": "LRP8",
          "gene_hgnc_id": 6700,
          "hgvs_c": "c.840C>A",
          "hgvs_p": "p.Gly280Gly",
          "transcript": "ENST00000668071.1",
          "protein_id": "ENSP00000499744.1",
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          "aa_end": null,
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          "cdna_start": 841,
          "cdna_end": null,
          "cdna_length": 3770,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LRP8",
          "gene_hgnc_id": 6700,
          "hgvs_c": "c.741C>A",
          "hgvs_p": "p.Gly247Gly",
          "transcript": "ENST00000662604.1",
          "protein_id": "ENSP00000499486.1",
          "transcript_support_level": null,
          "aa_start": 247,
          "aa_end": null,
          "aa_length": 732,
          "cds_start": 741,
          "cds_end": null,
          "cds_length": 2199,
          "cdna_start": 864,
          "cdna_end": null,
          "cdna_length": 2782,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LRP8",
          "gene_hgnc_id": 6700,
          "hgvs_c": "c.492C>A",
          "hgvs_p": "p.Gly164Gly",
          "transcript": "ENST00000658277.1",
          "protein_id": "ENSP00000499550.1",
          "transcript_support_level": null,
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          "cdna_start": 608,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 8,
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          "intron_rank": null,
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          "gene_symbol": "LRP8",
          "gene_hgnc_id": 6700,
          "hgvs_c": "c.870C>A",
          "hgvs_p": "p.Gly290Gly",
          "transcript": "NM_017522.5",
          "protein_id": "NP_059992.3",
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          "aa_end": null,
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          "cdna_start": 1028,
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          "biotype": null,
          "feature": null
        },
        {
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          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
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          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
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          "gene_symbol": "LRP8",
          "gene_hgnc_id": 6700,
          "hgvs_c": "c.387C>A",
          "hgvs_p": "p.Gly129Gly",
          "transcript": "ENST00000656486.1",
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          "cdna_start": 387,
          "cdna_end": null,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LRP8",
          "gene_hgnc_id": 6700,
          "hgvs_c": "c.30C>A",
          "hgvs_p": "p.Gly10Gly",
          "transcript": "ENST00000653169.1",
          "protein_id": "ENSP00000499783.1",
          "transcript_support_level": null,
          "aa_start": 10,
          "aa_end": null,
          "aa_length": 233,
          "cds_start": 30,
          "cds_end": null,
          "cds_length": 702,
          "cdna_start": 31,
          "cdna_end": null,
          "cdna_length": 1263,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LRP8",
          "gene_hgnc_id": 6700,
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          "effects": [
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      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
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  "message": null
}