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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: 11-44605090-T-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=44605090&ref=T&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "11",
"pos": 44605090,
"ref": "T",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_002231.4",
"consequences": [
{
"aa_ref": "Y",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CD82",
"gene_hgnc_id": 6210,
"hgvs_c": "c.169T>A",
"hgvs_p": "p.Tyr57Asn",
"transcript": "NM_002231.4",
"protein_id": "NP_002222.1",
"transcript_support_level": null,
"aa_start": 57,
"aa_end": null,
"aa_length": 267,
"cds_start": 169,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000227155.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_002231.4"
},
{
"aa_ref": "Y",
"aa_alt": "N",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CD82",
"gene_hgnc_id": 6210,
"hgvs_c": "c.169T>A",
"hgvs_p": "p.Tyr57Asn",
"transcript": "ENST00000227155.9",
"protein_id": "ENSP00000227155.4",
"transcript_support_level": 1,
"aa_start": 57,
"aa_end": null,
"aa_length": 267,
"cds_start": 169,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_002231.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000227155.9"
},
{
"aa_ref": "Y",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CD82",
"gene_hgnc_id": 6210,
"hgvs_c": "c.169T>A",
"hgvs_p": "p.Tyr57Asn",
"transcript": "ENST00000878578.1",
"protein_id": "ENSP00000548637.1",
"transcript_support_level": null,
"aa_start": 57,
"aa_end": null,
"aa_length": 314,
"cds_start": 169,
"cds_end": null,
"cds_length": 945,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878578.1"
},
{
"aa_ref": "Y",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CD82",
"gene_hgnc_id": 6210,
"hgvs_c": "c.169T>A",
"hgvs_p": "p.Tyr57Asn",
"transcript": "ENST00000878563.1",
"protein_id": "ENSP00000548622.1",
"transcript_support_level": null,
"aa_start": 57,
"aa_end": null,
"aa_length": 267,
"cds_start": 169,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878563.1"
},
{
"aa_ref": "Y",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CD82",
"gene_hgnc_id": 6210,
"hgvs_c": "c.169T>A",
"hgvs_p": "p.Tyr57Asn",
"transcript": "ENST00000878564.1",
"protein_id": "ENSP00000548623.1",
"transcript_support_level": null,
"aa_start": 57,
"aa_end": null,
"aa_length": 267,
"cds_start": 169,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878564.1"
},
{
"aa_ref": "Y",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CD82",
"gene_hgnc_id": 6210,
"hgvs_c": "c.169T>A",
"hgvs_p": "p.Tyr57Asn",
"transcript": "ENST00000878566.1",
"protein_id": "ENSP00000548625.1",
"transcript_support_level": null,
"aa_start": 57,
"aa_end": null,
"aa_length": 267,
"cds_start": 169,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878566.1"
},
{
"aa_ref": "Y",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CD82",
"gene_hgnc_id": 6210,
"hgvs_c": "c.169T>A",
"hgvs_p": "p.Tyr57Asn",
"transcript": "ENST00000878567.1",
"protein_id": "ENSP00000548626.1",
"transcript_support_level": null,
"aa_start": 57,
"aa_end": null,
"aa_length": 267,
"cds_start": 169,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878567.1"
},
{
"aa_ref": "Y",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CD82",
"gene_hgnc_id": 6210,
"hgvs_c": "c.169T>A",
"hgvs_p": "p.Tyr57Asn",
"transcript": "ENST00000878568.1",
"protein_id": "ENSP00000548627.1",
"transcript_support_level": null,
"aa_start": 57,
"aa_end": null,
"aa_length": 267,
"cds_start": 169,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878568.1"
},
{
"aa_ref": "Y",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CD82",
"gene_hgnc_id": 6210,
"hgvs_c": "c.169T>A",
"hgvs_p": "p.Tyr57Asn",
"transcript": "ENST00000878571.1",
"protein_id": "ENSP00000548630.1",
"transcript_support_level": null,
"aa_start": 57,
"aa_end": null,
"aa_length": 267,
"cds_start": 169,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878571.1"
},
{
"aa_ref": "Y",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CD82",
"gene_hgnc_id": 6210,
"hgvs_c": "c.169T>A",
"hgvs_p": "p.Tyr57Asn",
"transcript": "ENST00000878572.1",
"protein_id": "ENSP00000548631.1",
"transcript_support_level": null,
"aa_start": 57,
"aa_end": null,
"aa_length": 267,
"cds_start": 169,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878572.1"
},
{
"aa_ref": "Y",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CD82",
"gene_hgnc_id": 6210,
"hgvs_c": "c.169T>A",
"hgvs_p": "p.Tyr57Asn",
"transcript": "ENST00000878574.1",
"protein_id": "ENSP00000548633.1",
"transcript_support_level": null,
"aa_start": 57,
"aa_end": null,
"aa_length": 267,
"cds_start": 169,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878574.1"
},
{
"aa_ref": "Y",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CD82",
"gene_hgnc_id": 6210,
"hgvs_c": "c.169T>A",
"hgvs_p": "p.Tyr57Asn",
"transcript": "ENST00000878575.1",
"protein_id": "ENSP00000548634.1",
"transcript_support_level": null,
"aa_start": 57,
"aa_end": null,
"aa_length": 267,
"cds_start": 169,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878575.1"
},
{
"aa_ref": "Y",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CD82",
"gene_hgnc_id": 6210,
"hgvs_c": "c.169T>A",
"hgvs_p": "p.Tyr57Asn",
"transcript": "ENST00000878576.1",
"protein_id": "ENSP00000548635.1",
"transcript_support_level": null,
"aa_start": 57,
"aa_end": null,
"aa_length": 267,
"cds_start": 169,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878576.1"
},
{
"aa_ref": "Y",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CD82",
"gene_hgnc_id": 6210,
"hgvs_c": "c.169T>A",
"hgvs_p": "p.Tyr57Asn",
"transcript": "ENST00000878579.1",
"protein_id": "ENSP00000548638.1",
"transcript_support_level": null,
"aa_start": 57,
"aa_end": null,
"aa_length": 267,
"cds_start": 169,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878579.1"
},
{
"aa_ref": "Y",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CD82",
"gene_hgnc_id": 6210,
"hgvs_c": "c.169T>A",
"hgvs_p": "p.Tyr57Asn",
"transcript": "ENST00000878580.1",
"protein_id": "ENSP00000548639.1",
"transcript_support_level": null,
"aa_start": 57,
"aa_end": null,
"aa_length": 267,
"cds_start": 169,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878580.1"
},
{
"aa_ref": "Y",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CD82",
"gene_hgnc_id": 6210,
"hgvs_c": "c.169T>A",
"hgvs_p": "p.Tyr57Asn",
"transcript": "ENST00000878581.1",
"protein_id": "ENSP00000548640.1",
"transcript_support_level": null,
"aa_start": 57,
"aa_end": null,
"aa_length": 267,
"cds_start": 169,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878581.1"
},
{
"aa_ref": "Y",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CD82",
"gene_hgnc_id": 6210,
"hgvs_c": "c.169T>A",
"hgvs_p": "p.Tyr57Asn",
"transcript": "ENST00000878582.1",
"protein_id": "ENSP00000548641.1",
"transcript_support_level": null,
"aa_start": 57,
"aa_end": null,
"aa_length": 267,
"cds_start": 169,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000878582.1"
},
{
"aa_ref": "Y",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CD82",
"gene_hgnc_id": 6210,
"hgvs_c": "c.169T>A",
"hgvs_p": "p.Tyr57Asn",
"transcript": "ENST00000925720.1",
"protein_id": "ENSP00000595779.1",
"transcript_support_level": null,
"aa_start": 57,
"aa_end": null,
"aa_length": 267,
"cds_start": 169,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000925720.1"
},
{
"aa_ref": "Y",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CD82",
"gene_hgnc_id": 6210,
"hgvs_c": "c.169T>A",
"hgvs_p": "p.Tyr57Asn",
"transcript": "ENST00000968150.1",
"protein_id": "ENSP00000638209.1",
"transcript_support_level": null,
"aa_start": 57,
"aa_end": null,
"aa_length": 267,
"cds_start": 169,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968150.1"
},
{
"aa_ref": "Y",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CD82",
"gene_hgnc_id": 6210,
"hgvs_c": "c.169T>A",
"hgvs_p": "p.Tyr57Asn",
"transcript": "ENST00000968151.1",
"protein_id": "ENSP00000638210.1",
"transcript_support_level": null,
"aa_start": 57,
"aa_end": null,
"aa_length": 267,
"cds_start": 169,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968151.1"
},
{
"aa_ref": "Y",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CD82",
"gene_hgnc_id": 6210,
"hgvs_c": "c.169T>A",
"hgvs_p": "p.Tyr57Asn",
"transcript": "ENST00000968153.1",
"protein_id": "ENSP00000638212.1",
"transcript_support_level": null,
"aa_start": 57,
"aa_end": null,
"aa_length": 267,
"cds_start": 169,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968153.1"
},
{
"aa_ref": "Y",
"aa_alt": "N",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CD82",
"gene_hgnc_id": 6210,
"hgvs_c": "c.169T>A",
"hgvs_p": "p.Tyr57Asn",
"transcript": "ENST00000968155.1",
"protein_id": "ENSP00000638214.1",
"transcript_support_level": null,
"aa_start": 57,
"aa_end": null,
"aa_length": 267,
"cds_start": 169,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
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}