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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: 7-51028339-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=51028339&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "7",
"pos": 51028339,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_001410881.1",
"consequences": [
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COBL",
"gene_hgnc_id": 22199,
"hgvs_c": "c.2757C>G",
"hgvs_p": "p.His919Gln",
"transcript": "NM_015198.5",
"protein_id": "NP_056013.2",
"transcript_support_level": null,
"aa_start": 919,
"aa_end": null,
"aa_length": 1261,
"cds_start": 2757,
"cds_end": null,
"cds_length": 3786,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000265136.12",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_015198.5"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COBL",
"gene_hgnc_id": 22199,
"hgvs_c": "c.2757C>G",
"hgvs_p": "p.His919Gln",
"transcript": "ENST00000265136.12",
"protein_id": "ENSP00000265136.7",
"transcript_support_level": 1,
"aa_start": 919,
"aa_end": null,
"aa_length": 1261,
"cds_start": 2757,
"cds_end": null,
"cds_length": 3786,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_015198.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000265136.12"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COBL",
"gene_hgnc_id": 22199,
"hgvs_c": "c.3003C>G",
"hgvs_p": "p.His1001Gln",
"transcript": "ENST00000431948.6",
"protein_id": "ENSP00000413498.2",
"transcript_support_level": 1,
"aa_start": 1001,
"aa_end": null,
"aa_length": 1343,
"cds_start": 3003,
"cds_end": null,
"cds_length": 4032,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000431948.6"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COBL",
"gene_hgnc_id": 22199,
"hgvs_c": "c.2928C>G",
"hgvs_p": "p.His976Gln",
"transcript": "ENST00000395542.6",
"protein_id": "ENSP00000378912.3",
"transcript_support_level": 1,
"aa_start": 976,
"aa_end": null,
"aa_length": 1271,
"cds_start": 2928,
"cds_end": null,
"cds_length": 3816,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000395542.6"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COBL",
"gene_hgnc_id": 22199,
"hgvs_c": "c.2433C>G",
"hgvs_p": "p.His811Gln",
"transcript": "ENST00000445054.5",
"protein_id": "ENSP00000401204.1",
"transcript_support_level": 1,
"aa_start": 811,
"aa_end": null,
"aa_length": 1106,
"cds_start": 2433,
"cds_end": null,
"cds_length": 3321,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000445054.5"
},
{
"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": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COBL",
"gene_hgnc_id": 22199,
"hgvs_c": "n.6397C>G",
"hgvs_p": null,
"transcript": "ENST00000462395.1",
"protein_id": null,
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000462395.1"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COBL",
"gene_hgnc_id": 22199,
"hgvs_c": "c.3003C>G",
"hgvs_p": "p.His1001Gln",
"transcript": "NM_001410881.1",
"protein_id": "NP_001397810.1",
"transcript_support_level": null,
"aa_start": 1001,
"aa_end": null,
"aa_length": 1343,
"cds_start": 3003,
"cds_end": null,
"cds_length": 4032,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001410881.1"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COBL",
"gene_hgnc_id": 22199,
"hgvs_c": "c.2985C>G",
"hgvs_p": "p.His995Gln",
"transcript": "ENST00000902604.1",
"protein_id": "ENSP00000572663.1",
"transcript_support_level": null,
"aa_start": 995,
"aa_end": null,
"aa_length": 1337,
"cds_start": 2985,
"cds_end": null,
"cds_length": 4014,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000902604.1"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COBL",
"gene_hgnc_id": 22199,
"hgvs_c": "c.2910C>G",
"hgvs_p": "p.His970Gln",
"transcript": "ENST00000902602.1",
"protein_id": "ENSP00000572661.1",
"transcript_support_level": null,
"aa_start": 970,
"aa_end": null,
"aa_length": 1312,
"cds_start": 2910,
"cds_end": null,
"cds_length": 3939,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000902602.1"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COBL",
"gene_hgnc_id": 22199,
"hgvs_c": "c.3003C>G",
"hgvs_p": "p.His1001Gln",
"transcript": "ENST00000902598.1",
"protein_id": "ENSP00000572657.1",
"transcript_support_level": null,
"aa_start": 1001,
"aa_end": null,
"aa_length": 1296,
"cds_start": 3003,
"cds_end": null,
"cds_length": 3891,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000902598.1"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COBL",
"gene_hgnc_id": 22199,
"hgvs_c": "c.2985C>G",
"hgvs_p": "p.His995Gln",
"transcript": "ENST00000902599.1",
"protein_id": "ENSP00000572658.1",
"transcript_support_level": null,
"aa_start": 995,
"aa_end": null,
"aa_length": 1290,
"cds_start": 2985,
"cds_end": null,
"cds_length": 3873,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000902599.1"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COBL",
"gene_hgnc_id": 22199,
"hgvs_c": "c.2832C>G",
"hgvs_p": "p.His944Gln",
"transcript": "ENST00000902601.1",
"protein_id": "ENSP00000572660.1",
"transcript_support_level": null,
"aa_start": 944,
"aa_end": null,
"aa_length": 1286,
"cds_start": 2832,
"cds_end": null,
"cds_length": 3861,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000902601.1"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COBL",
"gene_hgnc_id": 22199,
"hgvs_c": "c.2802C>G",
"hgvs_p": "p.His934Gln",
"transcript": "ENST00000961292.1",
"protein_id": "ENSP00000631351.1",
"transcript_support_level": null,
"aa_start": 934,
"aa_end": null,
"aa_length": 1276,
"cds_start": 2802,
"cds_end": null,
"cds_length": 3831,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000961292.1"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COBL",
"gene_hgnc_id": 22199,
"hgvs_c": "c.2928C>G",
"hgvs_p": "p.His976Gln",
"transcript": "NM_001287436.3",
"protein_id": "NP_001274365.1",
"transcript_support_level": null,
"aa_start": 976,
"aa_end": null,
"aa_length": 1271,
"cds_start": 2928,
"cds_end": null,
"cds_length": 3816,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001287436.3"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COBL",
"gene_hgnc_id": 22199,
"hgvs_c": "c.2910C>G",
"hgvs_p": "p.His970Gln",
"transcript": "ENST00000902597.1",
"protein_id": "ENSP00000572656.1",
"transcript_support_level": null,
"aa_start": 970,
"aa_end": null,
"aa_length": 1265,
"cds_start": 2910,
"cds_end": null,
"cds_length": 3798,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000902597.1"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COBL",
"gene_hgnc_id": 22199,
"hgvs_c": "c.3003C>G",
"hgvs_p": "p.His1001Gln",
"transcript": "ENST00000902600.1",
"protein_id": "ENSP00000572659.1",
"transcript_support_level": null,
"aa_start": 1001,
"aa_end": null,
"aa_length": 1255,
"cds_start": 3003,
"cds_end": null,
"cds_length": 3768,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000902600.1"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COBL",
"gene_hgnc_id": 22199,
"hgvs_c": "c.2928C>G",
"hgvs_p": "p.His976Gln",
"transcript": "NM_001346441.2",
"protein_id": "NP_001333370.1",
"transcript_support_level": null,
"aa_start": 976,
"aa_end": null,
"aa_length": 1230,
"cds_start": 2928,
"cds_end": null,
"cds_length": 3693,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001346441.2"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COBL",
"gene_hgnc_id": 22199,
"hgvs_c": "c.2802C>G",
"hgvs_p": "p.His934Gln",
"transcript": "ENST00000961289.1",
"protein_id": "ENSP00000631348.1",
"transcript_support_level": null,
"aa_start": 934,
"aa_end": null,
"aa_length": 1229,
"cds_start": 2802,
"cds_end": null,
"cds_length": 3690,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000961289.1"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COBL",
"gene_hgnc_id": 22199,
"hgvs_c": "c.2757C>G",
"hgvs_p": "p.His919Gln",
"transcript": "NM_001346442.2",
"protein_id": "NP_001333371.1",
"transcript_support_level": null,
"aa_start": 919,
"aa_end": null,
"aa_length": 1214,
"cds_start": 2757,
"cds_end": null,
"cds_length": 3645,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001346442.2"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COBL",
"gene_hgnc_id": 22199,
"hgvs_c": "c.2757C>G",
"hgvs_p": "p.His919Gln",
"transcript": "ENST00000902594.1",
"protein_id": "ENSP00000572653.1",
"transcript_support_level": null,
"aa_start": 919,
"aa_end": null,
"aa_length": 1214,
"cds_start": 2757,
"cds_end": null,
"cds_length": 3645,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000902594.1"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COBL",
"gene_hgnc_id": 22199,
"hgvs_c": "c.2583C>G",
"hgvs_p": "p.His861Gln",
"transcript": "ENST00000902596.1",
"protein_id": "ENSP00000572655.1",
"transcript_support_level": null,
"aa_start": 861,
"aa_end": null,
"aa_length": 1203,
"cds_start": 2583,
"cds_end": null,
"cds_length": 3612,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000902596.1"
},
{
"aa_ref": "H",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "COBL",
"gene_hgnc_id": 22199,
"hgvs_c": "c.2802C>G",
"hgvs_p": "p.His934Gln",
"transcript": "ENST00000961290.1",
"protein_id": "ENSP00000631349.1",
"transcript_support_level": null,
"aa_start": 934,
"aa_end": null,
"aa_length": 1188,
"cds_start": 2802,
"cds_end": null,
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