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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: 17-13000202-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=13000202&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "17",
      "pos": 13000202,
      "ref": "G",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "NM_018127.7",
      "consequences": [
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELAC2",
          "gene_hgnc_id": 14198,
          "hgvs_c": "c.1377C>T",
          "hgvs_p": "p.Ser459Ser",
          "transcript": "NM_018127.7",
          "protein_id": "NP_060597.4",
          "transcript_support_level": null,
          "aa_start": 459,
          "aa_end": null,
          "aa_length": 826,
          "cds_start": 1377,
          "cds_end": null,
          "cds_length": 2481,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000338034.9",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_018127.7"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELAC2",
          "gene_hgnc_id": 14198,
          "hgvs_c": "c.1377C>T",
          "hgvs_p": "p.Ser459Ser",
          "transcript": "ENST00000338034.9",
          "protein_id": "ENSP00000337445.4",
          "transcript_support_level": 1,
          "aa_start": 459,
          "aa_end": null,
          "aa_length": 826,
          "cds_start": 1377,
          "cds_end": null,
          "cds_length": 2481,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_018127.7",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000338034.9"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELAC2",
          "gene_hgnc_id": 14198,
          "hgvs_c": "c.714C>T",
          "hgvs_p": "p.Ser238Ser",
          "transcript": "ENST00000446899.5",
          "protein_id": "ENSP00000406192.1",
          "transcript_support_level": 5,
          "aa_start": 238,
          "aa_end": null,
          "aa_length": 284,
          "cds_start": 714,
          "cds_end": null,
          "cds_length": 857,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000446899.5"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELAC2",
          "gene_hgnc_id": 14198,
          "hgvs_c": "c.1479C>T",
          "hgvs_p": "p.Ser493Ser",
          "transcript": "ENST00000923774.1",
          "protein_id": "ENSP00000593833.1",
          "transcript_support_level": null,
          "aa_start": 493,
          "aa_end": null,
          "aa_length": 860,
          "cds_start": 1479,
          "cds_end": null,
          "cds_length": 2583,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000923774.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELAC2",
          "gene_hgnc_id": 14198,
          "hgvs_c": "c.1401C>T",
          "hgvs_p": "p.Ser467Ser",
          "transcript": "ENST00000860253.1",
          "protein_id": "ENSP00000530312.1",
          "transcript_support_level": null,
          "aa_start": 467,
          "aa_end": null,
          "aa_length": 834,
          "cds_start": 1401,
          "cds_end": null,
          "cds_length": 2505,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000860253.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELAC2",
          "gene_hgnc_id": 14198,
          "hgvs_c": "c.1389C>T",
          "hgvs_p": "p.Ser463Ser",
          "transcript": "ENST00000923773.1",
          "protein_id": "ENSP00000593832.1",
          "transcript_support_level": null,
          "aa_start": 463,
          "aa_end": null,
          "aa_length": 830,
          "cds_start": 1389,
          "cds_end": null,
          "cds_length": 2493,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000923773.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELAC2",
          "gene_hgnc_id": 14198,
          "hgvs_c": "c.1383C>T",
          "hgvs_p": "p.Ser461Ser",
          "transcript": "ENST00000923771.1",
          "protein_id": "ENSP00000593830.1",
          "transcript_support_level": null,
          "aa_start": 461,
          "aa_end": null,
          "aa_length": 828,
          "cds_start": 1383,
          "cds_end": null,
          "cds_length": 2487,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000923771.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELAC2",
          "gene_hgnc_id": 14198,
          "hgvs_c": "c.1377C>T",
          "hgvs_p": "p.Ser459Ser",
          "transcript": "ENST00000860251.1",
          "protein_id": "ENSP00000530310.1",
          "transcript_support_level": null,
          "aa_start": 459,
          "aa_end": null,
          "aa_length": 827,
          "cds_start": 1377,
          "cds_end": null,
          "cds_length": 2484,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000860251.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELAC2",
          "gene_hgnc_id": 14198,
          "hgvs_c": "c.1374C>T",
          "hgvs_p": "p.Ser458Ser",
          "transcript": "ENST00000860249.1",
          "protein_id": "ENSP00000530308.1",
          "transcript_support_level": null,
          "aa_start": 458,
          "aa_end": null,
          "aa_length": 826,
          "cds_start": 1374,
          "cds_end": null,
          "cds_length": 2481,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000860249.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELAC2",
          "gene_hgnc_id": 14198,
          "hgvs_c": "c.1374C>T",
          "hgvs_p": "p.Ser458Ser",
          "transcript": "NM_173717.2",
          "protein_id": "NP_776065.1",
          "transcript_support_level": null,
          "aa_start": 458,
          "aa_end": null,
          "aa_length": 825,
          "cds_start": 1374,
          "cds_end": null,
          "cds_length": 2478,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_173717.2"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELAC2",
          "gene_hgnc_id": 14198,
          "hgvs_c": "c.1374C>T",
          "hgvs_p": "p.Ser458Ser",
          "transcript": "ENST00000860246.1",
          "protein_id": "ENSP00000530305.1",
          "transcript_support_level": null,
          "aa_start": 458,
          "aa_end": null,
          "aa_length": 825,
          "cds_start": 1374,
          "cds_end": null,
          "cds_length": 2478,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000860246.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELAC2",
          "gene_hgnc_id": 14198,
          "hgvs_c": "c.1377C>T",
          "hgvs_p": "p.Ser459Ser",
          "transcript": "ENST00000860247.1",
          "protein_id": "ENSP00000530306.1",
          "transcript_support_level": null,
          "aa_start": 459,
          "aa_end": null,
          "aa_length": 824,
          "cds_start": 1377,
          "cds_end": null,
          "cds_length": 2475,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000860247.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELAC2",
          "gene_hgnc_id": 14198,
          "hgvs_c": "c.1377C>T",
          "hgvs_p": "p.Ser459Ser",
          "transcript": "ENST00000961321.1",
          "protein_id": "ENSP00000631380.1",
          "transcript_support_level": null,
          "aa_start": 459,
          "aa_end": null,
          "aa_length": 824,
          "cds_start": 1377,
          "cds_end": null,
          "cds_length": 2475,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000961321.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELAC2",
          "gene_hgnc_id": 14198,
          "hgvs_c": "c.1374C>T",
          "hgvs_p": "p.Ser458Ser",
          "transcript": "ENST00000923772.1",
          "protein_id": "ENSP00000593831.1",
          "transcript_support_level": null,
          "aa_start": 458,
          "aa_end": null,
          "aa_length": 823,
          "cds_start": 1374,
          "cds_end": null,
          "cds_length": 2472,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000923772.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELAC2",
          "gene_hgnc_id": 14198,
          "hgvs_c": "c.1356C>T",
          "hgvs_p": "p.Ser452Ser",
          "transcript": "ENST00000961322.1",
          "protein_id": "ENSP00000631381.1",
          "transcript_support_level": null,
          "aa_start": 452,
          "aa_end": null,
          "aa_length": 819,
          "cds_start": 1356,
          "cds_end": null,
          "cds_length": 2460,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000961322.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELAC2",
          "gene_hgnc_id": 14198,
          "hgvs_c": "c.1377C>T",
          "hgvs_p": "p.Ser459Ser",
          "transcript": "ENST00000923775.1",
          "protein_id": "ENSP00000593834.1",
          "transcript_support_level": null,
          "aa_start": 459,
          "aa_end": null,
          "aa_length": 813,
          "cds_start": 1377,
          "cds_end": null,
          "cds_length": 2442,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000923775.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELAC2",
          "gene_hgnc_id": 14198,
          "hgvs_c": "c.1377C>T",
          "hgvs_p": "p.Ser459Ser",
          "transcript": "ENST00000860250.1",
          "protein_id": "ENSP00000530309.1",
          "transcript_support_level": null,
          "aa_start": 459,
          "aa_end": null,
          "aa_length": 812,
          "cds_start": 1377,
          "cds_end": null,
          "cds_length": 2439,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000860250.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELAC2",
          "gene_hgnc_id": 14198,
          "hgvs_c": "c.1374C>T",
          "hgvs_p": "p.Ser458Ser",
          "transcript": "ENST00000860254.1",
          "protein_id": "ENSP00000530313.1",
          "transcript_support_level": null,
          "aa_start": 458,
          "aa_end": null,
          "aa_length": 811,
          "cds_start": 1374,
          "cds_end": null,
          "cds_length": 2436,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000860254.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELAC2",
          "gene_hgnc_id": 14198,
          "hgvs_c": "c.1320C>T",
          "hgvs_p": "p.Ser440Ser",
          "transcript": "ENST00000395962.6",
          "protein_id": "ENSP00000379291.1",
          "transcript_support_level": 2,
          "aa_start": 440,
          "aa_end": null,
          "aa_length": 807,
          "cds_start": 1320,
          "cds_end": null,
          "cds_length": 2424,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000395962.6"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ELAC2",
          "gene_hgnc_id": 14198,
          "hgvs_c": "c.1377C>T",
          "hgvs_p": "p.Ser459Ser",
          "transcript": "ENST00000860252.1",
          "protein_id": "ENSP00000530311.1",
          "transcript_support_level": null,
          "aa_start": 459,
          "aa_end": null,
          "aa_length": 804,
          "cds_start": 1377,
          "cds_end": null,
          "cds_length": 2415,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
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            "synonymous_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.1377C>T",
          "hgvs_p": "p.Ser459Ser"
        }
      ],
      "clinvar_disease": "Combined oxidative phosphorylation defect type 17",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "Combined oxidative phosphorylation defect type 17",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}