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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: 16-50776244-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=16&pos=50776244&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "16",
"pos": 50776244,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "ENST00000427738.8",
"consequences": [
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CYLD",
"gene_hgnc_id": 2584,
"hgvs_c": "c.988G>A",
"hgvs_p": "p.Gly330Ser",
"transcript": "NM_001378743.1",
"protein_id": "NP_001365672.1",
"transcript_support_level": null,
"aa_start": 330,
"aa_end": null,
"aa_length": 956,
"cds_start": 988,
"cds_end": null,
"cds_length": 2871,
"cdna_start": 1230,
"cdna_end": null,
"cdna_length": 8540,
"mane_select": "ENST00000427738.8",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CYLD",
"gene_hgnc_id": 2584,
"hgvs_c": "c.988G>A",
"hgvs_p": "p.Gly330Ser",
"transcript": "ENST00000427738.8",
"protein_id": "ENSP00000392025.3",
"transcript_support_level": 5,
"aa_start": 330,
"aa_end": null,
"aa_length": 956,
"cds_start": 988,
"cds_end": null,
"cds_length": 2871,
"cdna_start": 1230,
"cdna_end": null,
"cdna_length": 8540,
"mane_select": "NM_001378743.1",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CYLD",
"gene_hgnc_id": 2584,
"hgvs_c": "c.979G>A",
"hgvs_p": "p.Gly327Ser",
"transcript": "ENST00000398568.6",
"protein_id": "ENSP00000381574.2",
"transcript_support_level": 1,
"aa_start": 327,
"aa_end": null,
"aa_length": 953,
"cds_start": 979,
"cds_end": null,
"cds_length": 2862,
"cdna_start": 1279,
"cdna_end": null,
"cdna_length": 3536,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CYLD",
"gene_hgnc_id": 2584,
"hgvs_c": "c.979G>A",
"hgvs_p": "p.Gly327Ser",
"transcript": "ENST00000569418.5",
"protein_id": "ENSP00000457576.1",
"transcript_support_level": 1,
"aa_start": 327,
"aa_end": null,
"aa_length": 953,
"cds_start": 979,
"cds_end": null,
"cds_length": 2862,
"cdna_start": 1257,
"cdna_end": null,
"cdna_length": 3513,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CYLD",
"gene_hgnc_id": 2584,
"hgvs_c": "c.979G>A",
"hgvs_p": "p.Gly327Ser",
"transcript": "ENST00000566206.5",
"protein_id": "ENSP00000462134.1",
"transcript_support_level": 1,
"aa_start": 327,
"aa_end": null,
"aa_length": 910,
"cds_start": 979,
"cds_end": null,
"cds_length": 2733,
"cdna_start": 1229,
"cdna_end": null,
"cdna_length": 3104,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CYLD",
"gene_hgnc_id": 2584,
"hgvs_c": "n.1374G>A",
"hgvs_p": null,
"transcript": "ENST00000569891.5",
"protein_id": null,
"transcript_support_level": 1,
"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": 4665,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CYLD",
"gene_hgnc_id": 2584,
"hgvs_c": "c.988G>A",
"hgvs_p": "p.Gly330Ser",
"transcript": "NM_015247.3",
"protein_id": "NP_056062.1",
"transcript_support_level": null,
"aa_start": 330,
"aa_end": null,
"aa_length": 956,
"cds_start": 988,
"cds_end": null,
"cds_length": 2871,
"cdna_start": 1367,
"cdna_end": null,
"cdna_length": 8677,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CYLD",
"gene_hgnc_id": 2584,
"hgvs_c": "c.988G>A",
"hgvs_p": "p.Gly330Ser",
"transcript": "ENST00000311559.13",
"protein_id": "ENSP00000308928.9",
"transcript_support_level": 5,
"aa_start": 330,
"aa_end": null,
"aa_length": 956,
"cds_start": 988,
"cds_end": null,
"cds_length": 2871,
"cdna_start": 1379,
"cdna_end": null,
"cdna_length": 5371,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CYLD",
"gene_hgnc_id": 2584,
"hgvs_c": "c.979G>A",
"hgvs_p": "p.Gly327Ser",
"transcript": "NM_001042355.2",
"protein_id": "NP_001035814.1",
"transcript_support_level": null,
"aa_start": 327,
"aa_end": null,
"aa_length": 953,
"cds_start": 979,
"cds_end": null,
"cds_length": 2862,
"cdna_start": 1221,
"cdna_end": null,
"cdna_length": 8531,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CYLD",
"gene_hgnc_id": 2584,
"hgvs_c": "c.979G>A",
"hgvs_p": "p.Gly327Ser",
"transcript": "NM_001042412.3",
"protein_id": "NP_001035877.1",
"transcript_support_level": null,
"aa_start": 327,
"aa_end": null,
"aa_length": 953,
"cds_start": 979,
"cds_end": null,
"cds_length": 2862,
"cdna_start": 1243,
"cdna_end": null,
"cdna_length": 8553,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CYLD",
"gene_hgnc_id": 2584,
"hgvs_c": "c.979G>A",
"hgvs_p": "p.Gly327Ser",
"transcript": "NM_001378744.1",
"protein_id": "NP_001365673.1",
"transcript_support_level": null,
"aa_start": 327,
"aa_end": null,
"aa_length": 953,
"cds_start": 979,
"cds_end": null,
"cds_length": 2862,
"cdna_start": 1248,
"cdna_end": null,
"cdna_length": 8558,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CYLD",
"gene_hgnc_id": 2584,
"hgvs_c": "c.979G>A",
"hgvs_p": "p.Gly327Ser",
"transcript": "NM_001378745.1",
"protein_id": "NP_001365674.1",
"transcript_support_level": null,
"aa_start": 327,
"aa_end": null,
"aa_length": 953,
"cds_start": 979,
"cds_end": null,
"cds_length": 2862,
"cdna_start": 1358,
"cdna_end": null,
"cdna_length": 8668,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CYLD",
"gene_hgnc_id": 2584,
"hgvs_c": "c.979G>A",
"hgvs_p": "p.Gly327Ser",
"transcript": "NM_001378746.1",
"protein_id": "NP_001365675.1",
"transcript_support_level": null,
"aa_start": 327,
"aa_end": null,
"aa_length": 953,
"cds_start": 979,
"cds_end": null,
"cds_length": 2862,
"cdna_start": 1380,
"cdna_end": null,
"cdna_length": 8690,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CYLD",
"gene_hgnc_id": 2584,
"hgvs_c": "c.979G>A",
"hgvs_p": "p.Gly327Ser",
"transcript": "NM_001378747.1",
"protein_id": "NP_001365676.1",
"transcript_support_level": null,
"aa_start": 327,
"aa_end": null,
"aa_length": 953,
"cds_start": 979,
"cds_end": null,
"cds_length": 2862,
"cdna_start": 1170,
"cdna_end": null,
"cdna_length": 8480,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CYLD",
"gene_hgnc_id": 2584,
"hgvs_c": "c.979G>A",
"hgvs_p": "p.Gly327Ser",
"transcript": "NM_001378748.1",
"protein_id": "NP_001365677.1",
"transcript_support_level": null,
"aa_start": 327,
"aa_end": null,
"aa_length": 953,
"cds_start": 979,
"cds_end": null,
"cds_length": 2862,
"cdna_start": 1430,
"cdna_end": null,
"cdna_length": 8740,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CYLD",
"gene_hgnc_id": 2584,
"hgvs_c": "c.979G>A",
"hgvs_p": "p.Gly327Ser",
"transcript": "NM_001378749.1",
"protein_id": "NP_001365678.1",
"transcript_support_level": null,
"aa_start": 327,
"aa_end": null,
"aa_length": 953,
"cds_start": 979,
"cds_end": null,
"cds_length": 2862,
"cdna_start": 1148,
"cdna_end": null,
"cdna_length": 8458,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CYLD",
"gene_hgnc_id": 2584,
"hgvs_c": "c.979G>A",
"hgvs_p": "p.Gly327Ser",
"transcript": "NM_001378750.1",
"protein_id": "NP_001365679.1",
"transcript_support_level": null,
"aa_start": 327,
"aa_end": null,
"aa_length": 953,
"cds_start": 979,
"cds_end": null,
"cds_length": 2862,
"cdna_start": 1567,
"cdna_end": null,
"cdna_length": 8877,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CYLD",
"gene_hgnc_id": 2584,
"hgvs_c": "c.979G>A",
"hgvs_p": "p.Gly327Ser",
"transcript": "ENST00000564326.5",
"protein_id": "ENSP00000454515.1",
"transcript_support_level": 5,
"aa_start": 327,
"aa_end": null,
"aa_length": 953,
"cds_start": 979,
"cds_end": null,
"cds_length": 2862,
"cdna_start": 1173,
"cdna_end": null,
"cdna_length": 3259,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CYLD",
"gene_hgnc_id": 2584,
"hgvs_c": "c.979G>A",
"hgvs_p": "p.Gly327Ser",
"transcript": "NM_001378751.1",
"protein_id": "NP_001365680.1",
"transcript_support_level": null,
"aa_start": 327,
"aa_end": null,
"aa_length": 943,
"cds_start": 979,
"cds_end": null,
"cds_length": 2832,
"cdna_start": 1221,
"cdna_end": null,
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"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CYLD",
"gene_hgnc_id": 2584,
"hgvs_c": "c.979G>A",
"hgvs_p": "p.Gly327Ser",
"transcript": "NM_001378752.1",
"protein_id": "NP_001365681.1",
"transcript_support_level": null,
"aa_start": 327,
"aa_end": null,
"aa_length": 943,
"cds_start": 979,
"cds_end": null,
"cds_length": 2832,
"cdna_start": 1243,
"cdna_end": null,
"cdna_length": 8523,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CYLD",
"gene_hgnc_id": 2584,
"hgvs_c": "c.979G>A",
"hgvs_p": "p.Gly327Ser",
"transcript": "NM_001378753.1",
"protein_id": "NP_001365682.1",
"transcript_support_level": null,
"aa_start": 327,
"aa_end": null,
"aa_length": 943,
"cds_start": 979,
"cds_end": null,
"cds_length": 2832,
"cdna_start": 1248,
"cdna_end": null,
"cdna_length": 8528,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CYLD",
"gene_hgnc_id": 2584,
"hgvs_c": "c.979G>A",
"hgvs_p": "p.Gly327Ser",
"transcript": "ENST00000568704.2",
"protein_id": "ENSP00000456488.2",
"transcript_support_level": 5,
"aa_start": 327,
"aa_end": null,
"aa_length": 771,
"cds_start": 979,
"cds_end": null,
"cds_length": 2316,
"cdna_start": 1129,
"cdna_end": null,
"cdna_length": 3292,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CYLD",
"gene_hgnc_id": 2584,
"hgvs_c": "c.313G>A",
"hgvs_p": "p.Gly105Ser",
"transcript": "NM_001378754.1",
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}