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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: 1-7809988-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=7809988&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "1",
      "pos": 7809988,
      "ref": "T",
      "alt": "C",
      "effect": "synonymous_variant",
      "transcript": "ENST00000377532.8",
      "consequences": [
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PER3",
          "gene_hgnc_id": 8847,
          "hgvs_c": "c.1338T>C",
          "hgvs_p": "p.Ser446Ser",
          "transcript": "NM_001377275.1",
          "protein_id": "NP_001364204.1",
          "transcript_support_level": null,
          "aa_start": 446,
          "aa_end": null,
          "aa_length": 1210,
          "cds_start": 1338,
          "cds_end": null,
          "cds_length": 3633,
          "cdna_start": 1648,
          "cdna_end": null,
          "cdna_length": 6365,
          "mane_select": "ENST00000377532.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PER3",
          "gene_hgnc_id": 8847,
          "hgvs_c": "c.1338T>C",
          "hgvs_p": "p.Ser446Ser",
          "transcript": "ENST00000377532.8",
          "protein_id": "ENSP00000366755.3",
          "transcript_support_level": 1,
          "aa_start": 446,
          "aa_end": null,
          "aa_length": 1210,
          "cds_start": 1338,
          "cds_end": null,
          "cds_length": 3633,
          "cdna_start": 1648,
          "cdna_end": null,
          "cdna_length": 6365,
          "mane_select": "NM_001377275.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PER3",
          "gene_hgnc_id": 8847,
          "hgvs_c": "c.1335T>C",
          "hgvs_p": "p.Ser445Ser",
          "transcript": "ENST00000361923.2",
          "protein_id": "ENSP00000355031.2",
          "transcript_support_level": 1,
          "aa_start": 445,
          "aa_end": null,
          "aa_length": 1201,
          "cds_start": 1335,
          "cds_end": null,
          "cds_length": 3606,
          "cdna_start": 1510,
          "cdna_end": null,
          "cdna_length": 6203,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PER3",
          "gene_hgnc_id": 8847,
          "hgvs_c": "c.1338T>C",
          "hgvs_p": "p.Ser446Ser",
          "transcript": "ENST00000614998.4",
          "protein_id": "ENSP00000479223.1",
          "transcript_support_level": 1,
          "aa_start": 446,
          "aa_end": null,
          "aa_length": 1191,
          "cds_start": 1338,
          "cds_end": null,
          "cds_length": 3576,
          "cdna_start": 1602,
          "cdna_end": null,
          "cdna_length": 6261,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PER3",
          "gene_hgnc_id": 8847,
          "hgvs_c": "c.1338T>C",
          "hgvs_p": "p.Ser446Ser",
          "transcript": "NM_001289862.2",
          "protein_id": "NP_001276791.1",
          "transcript_support_level": null,
          "aa_start": 446,
          "aa_end": null,
          "aa_length": 1210,
          "cds_start": 1338,
          "cds_end": null,
          "cds_length": 3633,
          "cdna_start": 1602,
          "cdna_end": null,
          "cdna_length": 6319,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PER3",
          "gene_hgnc_id": 8847,
          "hgvs_c": "c.1338T>C",
          "hgvs_p": "p.Ser446Ser",
          "transcript": "ENST00000613533.4",
          "protein_id": "ENSP00000482093.1",
          "transcript_support_level": 5,
          "aa_start": 446,
          "aa_end": null,
          "aa_length": 1210,
          "cds_start": 1338,
          "cds_end": null,
          "cds_length": 3633,
          "cdna_start": 1602,
          "cdna_end": null,
          "cdna_length": 6318,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PER3",
          "gene_hgnc_id": 8847,
          "hgvs_c": "c.1335T>C",
          "hgvs_p": "p.Ser445Ser",
          "transcript": "NM_001438696.1",
          "protein_id": "NP_001425625.1",
          "transcript_support_level": null,
          "aa_start": 445,
          "aa_end": null,
          "aa_length": 1209,
          "cds_start": 1335,
          "cds_end": null,
          "cds_length": 3630,
          "cdna_start": 1645,
          "cdna_end": null,
          "cdna_length": 6362,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PER3",
          "gene_hgnc_id": 8847,
          "hgvs_c": "c.1338T>C",
          "hgvs_p": "p.Ser446Ser",
          "transcript": "NM_001438697.1",
          "protein_id": "NP_001425626.1",
          "transcript_support_level": null,
          "aa_start": 446,
          "aa_end": null,
          "aa_length": 1209,
          "cds_start": 1338,
          "cds_end": null,
          "cds_length": 3630,
          "cdna_start": 1648,
          "cdna_end": null,
          "cdna_length": 6362,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PER3",
          "gene_hgnc_id": 8847,
          "hgvs_c": "c.1335T>C",
          "hgvs_p": "p.Ser445Ser",
          "transcript": "NM_001438698.1",
          "protein_id": "NP_001425627.1",
          "transcript_support_level": null,
          "aa_start": 445,
          "aa_end": null,
          "aa_length": 1208,
          "cds_start": 1335,
          "cds_end": null,
          "cds_length": 3627,
          "cdna_start": 1686,
          "cdna_end": null,
          "cdna_length": 6400,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PER3",
          "gene_hgnc_id": 8847,
          "hgvs_c": "c.1338T>C",
          "hgvs_p": "p.Ser446Ser",
          "transcript": "NM_001438700.1",
          "protein_id": "NP_001425629.1",
          "transcript_support_level": null,
          "aa_start": 446,
          "aa_end": null,
          "aa_length": 1203,
          "cds_start": 1338,
          "cds_end": null,
          "cds_length": 3612,
          "cdna_start": 1648,
          "cdna_end": null,
          "cdna_length": 6344,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PER3",
          "gene_hgnc_id": 8847,
          "hgvs_c": "c.1338T>C",
          "hgvs_p": "p.Ser446Ser",
          "transcript": "NM_001438701.1",
          "protein_id": "NP_001425630.1",
          "transcript_support_level": null,
          "aa_start": 446,
          "aa_end": null,
          "aa_length": 1203,
          "cds_start": 1338,
          "cds_end": null,
          "cds_length": 3612,
          "cdna_start": 1648,
          "cdna_end": null,
          "cdna_length": 6411,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PER3",
          "gene_hgnc_id": 8847,
          "hgvs_c": "c.1338T>C",
          "hgvs_p": "p.Ser446Ser",
          "transcript": "NM_001377276.1",
          "protein_id": "NP_001364205.1",
          "transcript_support_level": null,
          "aa_start": 446,
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          "aa_length": 1202,
          "cds_start": 1338,
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          "cds_length": 3609,
          "cdna_start": 1648,
          "cdna_end": null,
          "cdna_length": 6341,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
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          "gene_symbol": "PER3",
          "gene_hgnc_id": 8847,
          "hgvs_c": "c.1338T>C",
          "hgvs_p": "p.Ser446Ser",
          "transcript": "NM_001438702.1",
          "protein_id": "NP_001425631.1",
          "transcript_support_level": null,
          "aa_start": 446,
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          "aa_length": 1202,
          "cds_start": 1338,
          "cds_end": null,
          "cds_length": 3609,
          "cdna_start": 1648,
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          "cdna_length": 6408,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PER3",
          "gene_hgnc_id": 8847,
          "hgvs_c": "c.1335T>C",
          "hgvs_p": "p.Ser445Ser",
          "transcript": "NM_016831.4",
          "protein_id": "NP_058515.1",
          "transcript_support_level": null,
          "aa_start": 445,
          "aa_end": null,
          "aa_length": 1201,
          "cds_start": 1335,
          "cds_end": null,
          "cds_length": 3606,
          "cdna_start": 1737,
          "cdna_end": null,
          "cdna_length": 6430,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
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          "intron_rank": null,
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          "gene_symbol": "PER3",
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          "hgvs_c": "c.1338T>C",
          "hgvs_p": "p.Ser446Ser",
          "transcript": "NM_001438703.1",
          "protein_id": "NP_001425632.1",
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          "cdna_start": 1648,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PER3",
          "gene_hgnc_id": 8847,
          "hgvs_c": "c.1338T>C",
          "hgvs_p": "p.Ser446Ser",
          "transcript": "NM_001438704.1",
          "protein_id": "NP_001425633.1",
          "transcript_support_level": null,
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          "cds_start": 1338,
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          "cdna_start": 1648,
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          "cdna_length": 6387,
          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
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          "gene_symbol": "PER3",
          "gene_hgnc_id": 8847,
          "hgvs_c": "c.1335T>C",
          "hgvs_p": "p.Ser445Ser",
          "transcript": "NM_001438705.1",
          "protein_id": "NP_001425634.1",
          "transcript_support_level": null,
          "aa_start": 445,
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          "cdna_start": 1645,
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          "cdna_length": 6387,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
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          "intron_rank": null,
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          "gene_symbol": "PER3",
          "gene_hgnc_id": 8847,
          "hgvs_c": "c.1335T>C",
          "hgvs_p": "p.Ser445Ser",
          "transcript": "NM_001438706.1",
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        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
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          "intron_rank": null,
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          "gene_symbol": "PER3",
          "gene_hgnc_id": 8847,
          "hgvs_c": "c.1338T>C",
          "hgvs_p": "p.Ser446Ser",
          "transcript": "NM_001289861.2",
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        },
        {
          "aa_ref": "S",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
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          "intron_rank": null,
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          "gene_symbol": "PER3",
          "gene_hgnc_id": 8847,
          "hgvs_c": "c.1338T>C",
          "hgvs_p": "p.Ser446Ser",
          "transcript": "NM_001289863.3",
          "protein_id": "NP_001276792.1",
          "transcript_support_level": null,
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          "cds_length": 3555,
          "cdna_start": 1740,
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          "cdna_length": 6379,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
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          "gene_symbol": "PER3",
          "gene_hgnc_id": 8847,
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}