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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: 10-30845359-C-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=30845359&ref=C&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "10",
"pos": 30845359,
"ref": "C",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_182755.3",
"consequences": [
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF438",
"gene_hgnc_id": 21029,
"hgvs_c": "c.2089G>T",
"hgvs_p": "p.Ala697Ser",
"transcript": "NM_001143768.2",
"protein_id": "NP_001137240.1",
"transcript_support_level": null,
"aa_start": 697,
"aa_end": null,
"aa_length": 828,
"cds_start": 2089,
"cds_end": null,
"cds_length": 2487,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000436087.7",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001143768.2"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF438",
"gene_hgnc_id": 21029,
"hgvs_c": "c.2089G>T",
"hgvs_p": "p.Ala697Ser",
"transcript": "ENST00000436087.7",
"protein_id": "ENSP00000406934.2",
"transcript_support_level": 5,
"aa_start": 697,
"aa_end": null,
"aa_length": 828,
"cds_start": 2089,
"cds_end": null,
"cds_length": 2487,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001143768.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000436087.7"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF438",
"gene_hgnc_id": 21029,
"hgvs_c": "c.2089G>T",
"hgvs_p": "p.Ala697Ser",
"transcript": "ENST00000361310.7",
"protein_id": "ENSP00000354663.3",
"transcript_support_level": 1,
"aa_start": 697,
"aa_end": null,
"aa_length": 828,
"cds_start": 2089,
"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": "ENST00000361310.7"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF438",
"gene_hgnc_id": 21029,
"hgvs_c": "c.2059G>T",
"hgvs_p": "p.Ala687Ser",
"transcript": "ENST00000331737.10",
"protein_id": "ENSP00000333571.6",
"transcript_support_level": 1,
"aa_start": 687,
"aa_end": null,
"aa_length": 818,
"cds_start": 2059,
"cds_end": null,
"cds_length": 2457,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000331737.10"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF438",
"gene_hgnc_id": 21029,
"hgvs_c": "c.2089G>T",
"hgvs_p": "p.Ala697Ser",
"transcript": "NM_001143766.2",
"protein_id": "NP_001137238.1",
"transcript_support_level": null,
"aa_start": 697,
"aa_end": null,
"aa_length": 828,
"cds_start": 2089,
"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": "NM_001143766.2"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF438",
"gene_hgnc_id": 21029,
"hgvs_c": "c.2089G>T",
"hgvs_p": "p.Ala697Ser",
"transcript": "NM_001143767.2",
"protein_id": "NP_001137239.1",
"transcript_support_level": null,
"aa_start": 697,
"aa_end": null,
"aa_length": 828,
"cds_start": 2089,
"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": "NM_001143767.2"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF438",
"gene_hgnc_id": 21029,
"hgvs_c": "c.2089G>T",
"hgvs_p": "p.Ala697Ser",
"transcript": "NM_001387405.1",
"protein_id": "NP_001374334.1",
"transcript_support_level": null,
"aa_start": 697,
"aa_end": null,
"aa_length": 828,
"cds_start": 2089,
"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": "NM_001387405.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF438",
"gene_hgnc_id": 21029,
"hgvs_c": "c.2089G>T",
"hgvs_p": "p.Ala697Ser",
"transcript": "NM_001387411.1",
"protein_id": "NP_001374340.1",
"transcript_support_level": null,
"aa_start": 697,
"aa_end": null,
"aa_length": 828,
"cds_start": 2089,
"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": "NM_001387411.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF438",
"gene_hgnc_id": 21029,
"hgvs_c": "c.2089G>T",
"hgvs_p": "p.Ala697Ser",
"transcript": "NM_001387412.1",
"protein_id": "NP_001374341.1",
"transcript_support_level": null,
"aa_start": 697,
"aa_end": null,
"aa_length": 828,
"cds_start": 2089,
"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": "NM_001387412.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF438",
"gene_hgnc_id": 21029,
"hgvs_c": "c.2089G>T",
"hgvs_p": "p.Ala697Ser",
"transcript": "NM_182755.3",
"protein_id": "NP_877432.1",
"transcript_support_level": null,
"aa_start": 697,
"aa_end": null,
"aa_length": 828,
"cds_start": 2089,
"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": "NM_182755.3"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF438",
"gene_hgnc_id": 21029,
"hgvs_c": "c.2089G>T",
"hgvs_p": "p.Ala697Ser",
"transcript": "ENST00000413025.5",
"protein_id": "ENSP00000387546.1",
"transcript_support_level": 5,
"aa_start": 697,
"aa_end": null,
"aa_length": 828,
"cds_start": 2089,
"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": "ENST00000413025.5"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF438",
"gene_hgnc_id": 21029,
"hgvs_c": "c.2089G>T",
"hgvs_p": "p.Ala697Ser",
"transcript": "ENST00000442986.5",
"protein_id": "ENSP00000412363.1",
"transcript_support_level": 5,
"aa_start": 697,
"aa_end": null,
"aa_length": 828,
"cds_start": 2089,
"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": "ENST00000442986.5"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF438",
"gene_hgnc_id": 21029,
"hgvs_c": "c.2089G>T",
"hgvs_p": "p.Ala697Ser",
"transcript": "ENST00000885964.1",
"protein_id": "ENSP00000556023.1",
"transcript_support_level": null,
"aa_start": 697,
"aa_end": null,
"aa_length": 828,
"cds_start": 2089,
"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": "ENST00000885964.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF438",
"gene_hgnc_id": 21029,
"hgvs_c": "c.2089G>T",
"hgvs_p": "p.Ala697Ser",
"transcript": "ENST00000885965.1",
"protein_id": "ENSP00000556024.1",
"transcript_support_level": null,
"aa_start": 697,
"aa_end": null,
"aa_length": 828,
"cds_start": 2089,
"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": "ENST00000885965.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF438",
"gene_hgnc_id": 21029,
"hgvs_c": "c.2089G>T",
"hgvs_p": "p.Ala697Ser",
"transcript": "ENST00000885966.1",
"protein_id": "ENSP00000556025.1",
"transcript_support_level": null,
"aa_start": 697,
"aa_end": null,
"aa_length": 828,
"cds_start": 2089,
"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": "ENST00000885966.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF438",
"gene_hgnc_id": 21029,
"hgvs_c": "c.2089G>T",
"hgvs_p": "p.Ala697Ser",
"transcript": "ENST00000885967.1",
"protein_id": "ENSP00000556026.1",
"transcript_support_level": null,
"aa_start": 697,
"aa_end": null,
"aa_length": 828,
"cds_start": 2089,
"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": "ENST00000885967.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF438",
"gene_hgnc_id": 21029,
"hgvs_c": "c.2089G>T",
"hgvs_p": "p.Ala697Ser",
"transcript": "ENST00000885968.1",
"protein_id": "ENSP00000556027.1",
"transcript_support_level": null,
"aa_start": 697,
"aa_end": null,
"aa_length": 828,
"cds_start": 2089,
"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": "ENST00000885968.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF438",
"gene_hgnc_id": 21029,
"hgvs_c": "c.2089G>T",
"hgvs_p": "p.Ala697Ser",
"transcript": "ENST00000885969.1",
"protein_id": "ENSP00000556028.1",
"transcript_support_level": null,
"aa_start": 697,
"aa_end": null,
"aa_length": 828,
"cds_start": 2089,
"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": "ENST00000885969.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF438",
"gene_hgnc_id": 21029,
"hgvs_c": "c.2089G>T",
"hgvs_p": "p.Ala697Ser",
"transcript": "ENST00000885970.1",
"protein_id": "ENSP00000556029.1",
"transcript_support_level": null,
"aa_start": 697,
"aa_end": null,
"aa_length": 828,
"cds_start": 2089,
"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": "ENST00000885970.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF438",
"gene_hgnc_id": 21029,
"hgvs_c": "c.2089G>T",
"hgvs_p": "p.Ala697Ser",
"transcript": "ENST00000885971.1",
"protein_id": "ENSP00000556030.1",
"transcript_support_level": null,
"aa_start": 697,
"aa_end": null,
"aa_length": 828,
"cds_start": 2089,
"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": "ENST00000885971.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF438",
"gene_hgnc_id": 21029,
"hgvs_c": "c.2089G>T",
"hgvs_p": "p.Ala697Ser",
"transcript": "ENST00000885972.1",
"protein_id": "ENSP00000556031.1",
"transcript_support_level": null,
"aa_start": 697,
"aa_end": null,
"aa_length": 828,
"cds_start": 2089,
"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": "ENST00000885972.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF438",
"gene_hgnc_id": 21029,
"hgvs_c": "c.2089G>T",
"hgvs_p": "p.Ala697Ser",
"transcript": "ENST00000885973.1",
"protein_id": "ENSP00000556032.1",
"transcript_support_level": null,
"aa_start": 697,
"aa_end": null,
"aa_length": 828,
"cds_start": 2089,
"cds_end": null,
"cds_length": 2487,
"cdna_start": null,
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{
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}
],
"message": null
}