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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: 11-70470286-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=70470286&ref=A&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 70470286,
      "ref": "A",
      "alt": "G",
      "effect": "3_prime_UTR_variant",
      "transcript": "NM_012309.5",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SHANK2",
          "gene_hgnc_id": 14295,
          "hgvs_c": "c.*2583T>C",
          "hgvs_p": null,
          "transcript": "NM_012309.5",
          "protein_id": "NP_036441.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1849,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5550,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 10830,
          "mane_select": "ENST00000601538.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SHANK2",
          "gene_hgnc_id": 14295,
          "hgvs_c": "c.*2583T>C",
          "hgvs_p": null,
          "transcript": "ENST00000601538.6",
          "protein_id": "ENSP00000469689.2",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1849,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5550,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 10830,
          "mane_select": "NM_012309.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SHANK2",
          "gene_hgnc_id": 14295,
          "hgvs_c": "c.*2583T>C",
          "hgvs_p": null,
          "transcript": "ENST00000409161.5",
          "protein_id": "ENSP00000386491.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1253,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3762,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 9208,
          "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": "SHANK2",
          "gene_hgnc_id": 14295,
          "hgvs_c": "n.4885T>C",
          "hgvs_p": null,
          "transcript": "ENST00000606715.3",
          "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": 5738,
          "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": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SHANK2",
          "gene_hgnc_id": 14295,
          "hgvs_c": "n.3988T>C",
          "hgvs_p": null,
          "transcript": "NR_110766.2",
          "protein_id": null,
          "transcript_support_level": null,
          "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": 6420,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SHANK2",
          "gene_hgnc_id": 14295,
          "hgvs_c": "c.*2583T>C",
          "hgvs_p": null,
          "transcript": "NM_001441024.1",
          "protein_id": "NP_001427953.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1889,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5670,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 10950,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 23,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SHANK2",
          "gene_hgnc_id": 14295,
          "hgvs_c": "c.*2583T>C",
          "hgvs_p": null,
          "transcript": "NM_001441025.1",
          "protein_id": "NP_001427954.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1832,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5499,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 10779,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SHANK2",
          "gene_hgnc_id": 14295,
          "hgvs_c": "c.*2583T>C",
          "hgvs_p": null,
          "transcript": "NM_001441026.1",
          "protein_id": "NP_001427955.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1832,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 5499,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 10906,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SHANK2",
          "gene_hgnc_id": 14295,
          "hgvs_c": "c.*2583T>C",
          "hgvs_p": null,
          "transcript": "NM_001441027.1",
          "protein_id": "NP_001427956.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1832,
          "cds_start": -4,
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          "cds_length": 5499,
          "cdna_start": null,
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          "cdna_length": 11039,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 23,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SHANK2",
          "gene_hgnc_id": 14295,
          "hgvs_c": "c.*2583T>C",
          "hgvs_p": null,
          "transcript": "NM_001441028.1",
          "protein_id": "NP_001427957.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1832,
          "cds_start": -4,
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          "cds_length": 5499,
          "cdna_start": null,
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          "cdna_length": 10903,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
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          "gene_symbol": "SHANK2",
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          "hgvs_c": "c.*2583T>C",
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          "transcript": "NM_001441029.1",
          "protein_id": "NP_001427958.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 1832,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 10912,
          "mane_select": null,
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          "biotype": null,
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        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
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          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 23,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SHANK2",
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          "hgvs_c": "c.*2583T>C",
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          "consequences": [
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          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
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          "gene_symbol": "SHANK2",
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          "hgvs_c": "c.*2583T>C",
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        {
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          ],
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          "exon_count": 23,
          "intron_rank": null,
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          "gene_symbol": "SHANK2",
          "gene_hgnc_id": 14295,
          "hgvs_c": "c.*2583T>C",
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          "transcript": "NM_001441032.1",
          "protein_id": "NP_001427961.1",
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        },
        {
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          "consequences": [
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          ],
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          "intron_rank": null,
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          "gene_symbol": "SHANK2",
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          "exon_count": 22,
          "intron_rank": null,
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          "gene_symbol": "SHANK2",
          "gene_hgnc_id": 14295,
          "hgvs_c": "c.*2583T>C",
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          "transcript": "NM_001441034.1",
          "protein_id": "NP_001427963.1",
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        {
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          ],
          "exon_rank": 23,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
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          "gene_symbol": "SHANK2",
          "gene_hgnc_id": 14295,
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          "transcript": "NM_001441035.1",
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        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 24,
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          "exon_count": 24,
          "intron_rank": null,
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          "gene_symbol": "SHANK2",
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          "exon_count": 22,
          "intron_rank": null,
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          "gene_symbol": "SHANK2",
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          "hgvs_c": "c.*2583T>C",
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        {
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          "intron_rank": null,
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          "gene_symbol": "SHANK2",
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          "transcript": "NM_001441038.1",
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          "cdna_start": null,
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          "feature": null
        },
        {
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          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 24,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SHANK2",
          "gene_hgnc_id": 14295,
          "hgvs_c": "c.*3189T>C",
          "hgvs_p": null,
          "transcript": "NM_001441039.1",
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      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:2",
      "phenotype_combined": "Autism spectrum disorder|not provided",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
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  "message": null
}