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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: 20-44540989-G-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=20&pos=44540989&ref=G&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "20",
      "pos": 44540989,
      "ref": "G",
      "alt": "C",
      "effect": "intron_variant",
      "transcript": "NM_007066.5",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PKIG",
          "gene_hgnc_id": 9019,
          "hgvs_c": "c.-94+9011G>C",
          "hgvs_p": null,
          "transcript": "ENST00000372894.7",
          "protein_id": "ENSP00000361985.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 76,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 231,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000372894.7"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PKIG",
          "gene_hgnc_id": 9019,
          "hgvs_c": "c.-516+9011G>C",
          "hgvs_p": null,
          "transcript": "NM_001281444.2",
          "protein_id": "NP_001268373.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 76,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 231,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001281444.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PKIG",
          "gene_hgnc_id": 9019,
          "hgvs_c": "c.-94+9011G>C",
          "hgvs_p": null,
          "transcript": "NM_007066.5",
          "protein_id": "NP_008997.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 76,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 231,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_007066.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PKIG",
          "gene_hgnc_id": 9019,
          "hgvs_c": "c.-241+9011G>C",
          "hgvs_p": null,
          "transcript": "NM_181804.3",
          "protein_id": "NP_861520.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 76,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 231,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_181804.3"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PKIG",
          "gene_hgnc_id": 9019,
          "hgvs_c": "c.-346+9011G>C",
          "hgvs_p": null,
          "transcript": "NM_181805.3",
          "protein_id": "NP_861521.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 76,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 231,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_181805.3"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PKIG",
          "gene_hgnc_id": 9019,
          "hgvs_c": "c.-516+9011G>C",
          "hgvs_p": null,
          "transcript": "ENST00000372889.5",
          "protein_id": "ENSP00000361980.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 76,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 231,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000372889.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PKIG",
          "gene_hgnc_id": 9019,
          "hgvs_c": "c.-346+9011G>C",
          "hgvs_p": null,
          "transcript": "ENST00000372891.7",
          "protein_id": "ENSP00000361981.3",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 76,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 231,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000372891.7"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PKIG",
          "gene_hgnc_id": 9019,
          "hgvs_c": "c.-241+9011G>C",
          "hgvs_p": null,
          "transcript": "ENST00000372892.7",
          "protein_id": "ENSP00000361983.3",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 76,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 231,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000372892.7"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PKIG",
          "gene_hgnc_id": 9019,
          "hgvs_c": "c.-184+8589G>C",
          "hgvs_p": null,
          "transcript": "ENST00000902612.1",
          "protein_id": "ENSP00000572671.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 76,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 231,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000902612.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PKIG",
          "gene_hgnc_id": 9019,
          "hgvs_c": "c.-241+8589G>C",
          "hgvs_p": null,
          "transcript": "ENST00000902613.1",
          "protein_id": "ENSP00000572672.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 76,
          "cds_start": null,
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          "cds_length": 231,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000902613.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 1,
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          "gene_symbol": "PKIG",
          "gene_hgnc_id": 9019,
          "hgvs_c": "c.-369+9011G>C",
          "hgvs_p": null,
          "transcript": "ENST00000902615.1",
          "protein_id": "ENSP00000572674.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 76,
          "cds_start": null,
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          "cds_length": 231,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000902615.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PKIG",
          "gene_hgnc_id": 9019,
          "hgvs_c": "c.-24+9011G>C",
          "hgvs_p": null,
          "transcript": "ENST00000902616.1",
          "protein_id": "ENSP00000572675.1",
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          "cds_start": null,
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          "cdna_start": null,
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        {
          "aa_ref": null,
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          "protein_coding": true,
          "strand": true,
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          ],
          "exon_rank": null,
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          "hgvs_c": "c.-184+9011G>C",
          "hgvs_p": null,
          "transcript": "ENST00000902617.1",
          "protein_id": "ENSP00000572676.1",
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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": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "gene_symbol": "PKIG",
          "gene_hgnc_id": 9019,
          "hgvs_c": "c.-94+8589G>C",
          "hgvs_p": null,
          "transcript": "ENST00000902619.1",
          "protein_id": "ENSP00000572678.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 76,
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          "cdna_start": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000902619.1"
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
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          "hgvs_p": null,
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 5,
          "intron_rank": 1,
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          "gene_symbol": "PKIG",
          "gene_hgnc_id": 9019,
          "hgvs_c": "c.-199+9011G>C",
          "hgvs_p": null,
          "transcript": "ENST00000902621.1",
          "protein_id": "ENSP00000572680.1",
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 4,
          "intron_rank": 1,
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          "gene_symbol": "PKIG",
          "gene_hgnc_id": 9019,
          "hgvs_c": "c.-183+9011G>C",
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          "transcript": "ENST00000902623.1",
          "protein_id": "ENSP00000572682.1",
          "transcript_support_level": null,
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        {
          "aa_ref": null,
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          "gene_symbol": "PKIG",
          "gene_hgnc_id": 9019,
          "hgvs_c": "c.-1098+9011G>C",
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        {
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          "gene_symbol": "PKIG",
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          "hgvs_c": "c.-346+8589G>C",
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        },
        {
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          "canonical": false,
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          ],
          "exon_rank": null,
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          "exon_count": 4,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PKIG",
          "gene_hgnc_id": 9019,
          "hgvs_c": "c.-171+8589G>C",
          "hgvs_p": null,
          "transcript": "ENST00000902626.1",
          "protein_id": "ENSP00000572685.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_start": null,
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          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000902626.1"
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 1,
          "intron_rank_end": null,
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}