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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: 22-36155868-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=22&pos=36155868&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "22",
"pos": 36155868,
"ref": "C",
"alt": "T",
"effect": "intron_variant",
"transcript": "ENST00000424878.4",
"consequences": [
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "APOL3",
"gene_hgnc_id": 14868,
"hgvs_c": "c.-88+4801G>A",
"hgvs_p": null,
"transcript": "NM_145639.2",
"protein_id": "NP_663614.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 331,
"cds_start": -4,
"cds_end": null,
"cds_length": 996,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2041,
"mane_select": "ENST00000424878.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "APOL3",
"gene_hgnc_id": 14868,
"hgvs_c": "c.-88+4801G>A",
"hgvs_p": null,
"transcript": "ENST00000424878.4",
"protein_id": "ENSP00000415779.3",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 331,
"cds_start": -4,
"cds_end": null,
"cds_length": 996,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2041,
"mane_select": "NM_145639.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "APOL3",
"gene_hgnc_id": 14868,
"hgvs_c": "c.223+4801G>A",
"hgvs_p": null,
"transcript": "ENST00000349314.7",
"protein_id": "ENSP00000344577.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 402,
"cds_start": -4,
"cds_end": null,
"cds_length": 1209,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2655,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "APOL3",
"gene_hgnc_id": 14868,
"hgvs_c": "c.-378+4801G>A",
"hgvs_p": null,
"transcript": "ENST00000361710.6",
"protein_id": "ENSP00000355164.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 202,
"cds_start": -4,
"cds_end": null,
"cds_length": 609,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3563,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "APOL3",
"gene_hgnc_id": 14868,
"hgvs_c": "c.-378+4801G>A",
"hgvs_p": null,
"transcript": "ENST00000397287.6",
"protein_id": "ENSP00000380456.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 202,
"cds_start": -4,
"cds_end": null,
"cds_length": 609,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3626,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "APOL3",
"gene_hgnc_id": 14868,
"hgvs_c": "c.116-1240G>A",
"hgvs_p": null,
"transcript": "ENST00000531095.1",
"protein_id": "ENSP00000432271.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 40,
"cds_start": -4,
"cds_end": null,
"cds_length": 123,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 295,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "APOL3",
"gene_hgnc_id": 14868,
"hgvs_c": "n.223+4801G>A",
"hgvs_p": null,
"transcript": "ENST00000397289.6",
"protein_id": "ENSP00000380457.2",
"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": 2214,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "APOL3",
"gene_hgnc_id": 14868,
"hgvs_c": "n.223+4801G>A",
"hgvs_p": null,
"transcript": "ENST00000422426.5",
"protein_id": "ENSP00000409345.1",
"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": 2327,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "APOL3",
"gene_hgnc_id": 14868,
"hgvs_c": "n.223+4801G>A",
"hgvs_p": null,
"transcript": "ENST00000432700.5",
"protein_id": "ENSP00000416732.1",
"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": 2443,
"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": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "APOL3",
"gene_hgnc_id": 14868,
"hgvs_c": "n.213G>A",
"hgvs_p": null,
"transcript": "ENST00000528740.1",
"protein_id": null,
"transcript_support_level": 3,
"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": 361,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "APOL3",
"gene_hgnc_id": 14868,
"hgvs_c": "c.223+4801G>A",
"hgvs_p": null,
"transcript": "NM_145640.2",
"protein_id": "NP_663615.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 402,
"cds_start": -4,
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"cds_length": 1209,
"cdna_start": null,
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"cdna_length": 2124,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "APOL3",
"gene_hgnc_id": 14868,
"hgvs_c": "c.-317+3509G>A",
"hgvs_p": null,
"transcript": "NM_001393587.1",
"protein_id": "NP_001380516.1",
"transcript_support_level": null,
"aa_start": null,
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"cds_start": -4,
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"cdna_start": null,
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"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 5,
"intron_rank": 1,
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"gene_symbol": "APOL3",
"gene_hgnc_id": 14868,
"hgvs_c": "c.-201+4801G>A",
"hgvs_p": null,
"transcript": "NM_001393588.1",
"protein_id": "NP_001380517.1",
"transcript_support_level": null,
"aa_start": null,
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},
{
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"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "APOL3",
"gene_hgnc_id": 14868,
"hgvs_c": "c.-88+976G>A",
"hgvs_p": null,
"transcript": "NM_001393589.1",
"protein_id": "NP_001380518.1",
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},
{
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],
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"exon_count": 4,
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"gene_symbol": "APOL3",
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"hgvs_c": "c.-317+4801G>A",
"hgvs_p": null,
"transcript": "NM_001393590.1",
"protein_id": "NP_001380519.1",
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"feature": null
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "APOL3",
"gene_hgnc_id": 14868,
"hgvs_c": "c.-88+4801G>A",
"hgvs_p": null,
"transcript": "NM_001393591.1",
"protein_id": "NP_001380520.1",
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},
{
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],
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"gene_symbol": "APOL3",
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"hgvs_c": "c.-317+976G>A",
"hgvs_p": null,
"transcript": "NM_001393592.1",
"protein_id": "NP_001380521.1",
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"feature": null
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "APOL3",
"gene_hgnc_id": 14868,
"hgvs_c": "c.-131+976G>A",
"hgvs_p": null,
"transcript": "NM_001393593.1",
"protein_id": "NP_001380522.1",
"transcript_support_level": null,
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"cdna_start": null,
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"mane_select": null,
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"biotype": null,
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},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "APOL3",
"gene_hgnc_id": 14868,
"hgvs_c": "c.-244+4801G>A",
"hgvs_p": null,
"transcript": "NM_001393595.1",
"protein_id": "NP_001380524.1",
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},
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"consequences": [
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],
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"intron_rank": 2,
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"gene_symbol": "APOL3",
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"hgvs_c": "c.-201+3509G>A",
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},
{
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"strand": false,
"consequences": [
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],
"exon_rank": null,
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"intron_rank": 2,
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"gene_symbol": "APOL3",
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"hgvs_c": "c.-88+3509G>A",
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"transcript": "NM_001393597.1",
"protein_id": "NP_001380526.1",
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},
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"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "APOL3",
"gene_hgnc_id": 14868,
"hgvs_c": "c.-317+3509G>A",
"hgvs_p": null,
"transcript": "NM_001393598.1",
"protein_id": "NP_001380527.1",
"transcript_support_level": null,
"aa_start": null,
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"cds_start": -4,
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"cdna_start": null,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "APOL3",
"gene_hgnc_id": 14868,
"hgvs_c": "c.-131+4801G>A",
"hgvs_p": null,
"transcript": "NM_001393599.1",
"protein_id": "NP_001380528.1",
"transcript_support_level": null,
"aa_start": null,
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"mane_select": null,
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},
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}
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}