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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: 2-127428530-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=127428530&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 127428530,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_001375607.1",
"consequences": [
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PROC",
"gene_hgnc_id": 9451,
"hgvs_c": "c.970G>A",
"hgvs_p": "p.Gly324Ser",
"transcript": "NM_000312.4",
"protein_id": "NP_000303.1",
"transcript_support_level": null,
"aa_start": 324,
"aa_end": null,
"aa_length": 461,
"cds_start": 970,
"cds_end": null,
"cds_length": 1386,
"cdna_start": 1057,
"cdna_end": null,
"cdna_length": 1769,
"mane_select": "ENST00000234071.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_000312.4"
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PROC",
"gene_hgnc_id": 9451,
"hgvs_c": "c.970G>A",
"hgvs_p": "p.Gly324Ser",
"transcript": "ENST00000234071.8",
"protein_id": "ENSP00000234071.4",
"transcript_support_level": 1,
"aa_start": 324,
"aa_end": null,
"aa_length": 461,
"cds_start": 970,
"cds_end": null,
"cds_length": 1386,
"cdna_start": 1057,
"cdna_end": null,
"cdna_length": 1769,
"mane_select": "NM_000312.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000234071.8"
},
{
"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": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PROC",
"gene_hgnc_id": 9451,
"hgvs_c": "c.1156G>A",
"hgvs_p": "p.Gly386Ser",
"transcript": "NM_001375607.1",
"protein_id": "NP_001362536.1",
"transcript_support_level": null,
"aa_start": 386,
"aa_end": null,
"aa_length": 523,
"cds_start": 1156,
"cds_end": null,
"cds_length": 1572,
"cdna_start": 1176,
"cdna_end": null,
"cdna_length": 1888,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001375607.1"
},
{
"aa_ref": "G",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PROC",
"gene_hgnc_id": 9451,
"hgvs_c": "c.1153G>A",
"hgvs_p": "p.Gly385Ser",
"transcript": "NM_001375602.1",
"protein_id": "NP_001362531.1",
"transcript_support_level": null,
"aa_start": 385,
"aa_end": null,
"aa_length": 522,
"cds_start": 1153,
"cds_end": null,
"cds_length": 1569,
"cdna_start": 1173,
"cdna_end": null,
"cdna_length": 1885,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001375602.1"
},
{
"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": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PROC",
"gene_hgnc_id": 9451,
"hgvs_c": "c.1144G>A",
"hgvs_p": "p.Gly382Ser",
"transcript": "ENST00000883860.1",
"protein_id": "ENSP00000553919.1",
"transcript_support_level": null,
"aa_start": 382,
"aa_end": null,
"aa_length": 519,
"cds_start": 1144,
"cds_end": null,
"cds_length": 1560,
"cdna_start": 1238,
"cdna_end": null,
"cdna_length": 1721,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000883860.1"
},
{
"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": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PROC",
"gene_hgnc_id": 9451,
"hgvs_c": "c.1144G>A",
"hgvs_p": "p.Gly382Ser",
"transcript": "ENST00000883897.1",
"protein_id": "ENSP00000553956.1",
"transcript_support_level": null,
"aa_start": 382,
"aa_end": null,
"aa_length": 519,
"cds_start": 1144,
"cds_end": null,
"cds_length": 1560,
"cdna_start": 1433,
"cdna_end": null,
"cdna_length": 2118,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000883897.1"
},
{
"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": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PROC",
"gene_hgnc_id": 9451,
"hgvs_c": "c.1138G>A",
"hgvs_p": "p.Gly380Ser",
"transcript": "NM_001375606.1",
"protein_id": "NP_001362535.1",
"transcript_support_level": null,
"aa_start": 380,
"aa_end": null,
"aa_length": 517,
"cds_start": 1138,
"cds_end": null,
"cds_length": 1554,
"cdna_start": 1158,
"cdna_end": null,
"cdna_length": 1870,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001375606.1"
},
{
"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": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PROC",
"gene_hgnc_id": 9451,
"hgvs_c": "c.1135G>A",
"hgvs_p": "p.Gly379Ser",
"transcript": "NM_001375603.1",
"protein_id": "NP_001362532.1",
"transcript_support_level": null,
"aa_start": 379,
"aa_end": null,
"aa_length": 516,
"cds_start": 1135,
"cds_end": null,
"cds_length": 1551,
"cdna_start": 1155,
"cdna_end": null,
"cdna_length": 1867,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001375603.1"
},
{
"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": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PROC",
"gene_hgnc_id": 9451,
"hgvs_c": "c.1123G>A",
"hgvs_p": "p.Gly375Ser",
"transcript": "ENST00000883902.1",
"protein_id": "ENSP00000553961.1",
"transcript_support_level": null,
"aa_start": 375,
"aa_end": null,
"aa_length": 512,
"cds_start": 1123,
"cds_end": null,
"cds_length": 1539,
"cdna_start": 1369,
"cdna_end": null,
"cdna_length": 1853,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000883902.1"
},
{
"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": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PROC",
"gene_hgnc_id": 9451,
"hgvs_c": "c.1072G>A",
"hgvs_p": "p.Gly358Ser",
"transcript": "NM_001375605.1",
"protein_id": "NP_001362534.1",
"transcript_support_level": null,
"aa_start": 358,
"aa_end": null,
"aa_length": 495,
"cds_start": 1072,
"cds_end": null,
"cds_length": 1488,
"cdna_start": 1159,
"cdna_end": null,
"cdna_length": 1871,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001375605.1"
},
{
"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": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PROC",
"gene_hgnc_id": 9451,
"hgvs_c": "c.1072G>A",
"hgvs_p": "p.Gly358Ser",
"transcript": "ENST00000409048.1",
"protein_id": "ENSP00000386679.1",
"transcript_support_level": 5,
"aa_start": 358,
"aa_end": null,
"aa_length": 495,
"cds_start": 1072,
"cds_end": null,
"cds_length": 1488,
"cdna_start": 1133,
"cdna_end": null,
"cdna_length": 1586,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000409048.1"
},
{
"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": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PROC",
"gene_hgnc_id": 9451,
"hgvs_c": "c.1072G>A",
"hgvs_p": "p.Gly358Ser",
"transcript": "ENST00000883843.1",
"protein_id": "ENSP00000553902.1",
"transcript_support_level": null,
"aa_start": 358,
"aa_end": null,
"aa_length": 495,
"cds_start": 1072,
"cds_end": null,
"cds_length": 1488,
"cdna_start": 1266,
"cdna_end": null,
"cdna_length": 1984,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000883843.1"
},
{
"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": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PROC",
"gene_hgnc_id": 9451,
"hgvs_c": "c.1072G>A",
"hgvs_p": "p.Gly358Ser",
"transcript": "ENST00000883844.1",
"protein_id": "ENSP00000553903.1",
"transcript_support_level": null,
"aa_start": 358,
"aa_end": null,
"aa_length": 495,
"cds_start": 1072,
"cds_end": null,
"cds_length": 1488,
"cdna_start": 1262,
"cdna_end": null,
"cdna_length": 1980,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000883844.1"
},
{
"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": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PROC",
"gene_hgnc_id": 9451,
"hgvs_c": "c.1072G>A",
"hgvs_p": "p.Gly358Ser",
"transcript": "ENST00000883854.1",
"protein_id": "ENSP00000553913.1",
"transcript_support_level": null,
"aa_start": 358,
"aa_end": null,
"aa_length": 495,
"cds_start": 1072,
"cds_end": null,
"cds_length": 1488,
"cdna_start": 1170,
"cdna_end": null,
"cdna_length": 1855,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000883854.1"
},
{
"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": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PROC",
"gene_hgnc_id": 9451,
"hgvs_c": "c.1072G>A",
"hgvs_p": "p.Gly358Ser",
"transcript": "ENST00000883858.1",
"protein_id": "ENSP00000553917.1",
"transcript_support_level": null,
"aa_start": 358,
"aa_end": null,
"aa_length": 495,
"cds_start": 1072,
"cds_end": null,
"cds_length": 1488,
"cdna_start": 1436,
"cdna_end": null,
"cdna_length": 2151,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000883858.1"
},
{
"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": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PROC",
"gene_hgnc_id": 9451,
"hgvs_c": "c.1072G>A",
"hgvs_p": "p.Gly358Ser",
"transcript": "ENST00000883861.1",
"protein_id": "ENSP00000553920.1",
"transcript_support_level": null,
"aa_start": 358,
"aa_end": null,
"aa_length": 495,
"cds_start": 1072,
"cds_end": null,
"cds_length": 1488,
"cdna_start": 1178,
"cdna_end": null,
"cdna_length": 1661,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000883861.1"
},
{
"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": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PROC",
"gene_hgnc_id": 9451,
"hgvs_c": "c.1072G>A",
"hgvs_p": "p.Gly358Ser",
"transcript": "ENST00000883880.1",
"protein_id": "ENSP00000553939.1",
"transcript_support_level": null,
"aa_start": 358,
"aa_end": null,
"aa_length": 495,
"cds_start": 1072,
"cds_end": null,
"cds_length": 1488,
"cdna_start": 1381,
"cdna_end": null,
"cdna_length": 1865,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000883880.1"
},
{
"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": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PROC",
"gene_hgnc_id": 9451,
"hgvs_c": "c.1072G>A",
"hgvs_p": "p.Gly358Ser",
"transcript": "ENST00000883881.1",
"protein_id": "ENSP00000553940.1",
"transcript_support_level": null,
"aa_start": 358,
"aa_end": null,
"aa_length": 495,
"cds_start": 1072,
"cds_end": null,
"cds_length": 1488,
"cdna_start": 1269,
"cdna_end": null,
"cdna_length": 1984,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000883881.1"
},
{
"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": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PROC",
"gene_hgnc_id": 9451,
"hgvs_c": "c.1072G>A",
"hgvs_p": "p.Gly358Ser",
"transcript": "ENST00000883888.1",
"protein_id": "ENSP00000553947.1",
"transcript_support_level": null,
"aa_start": 358,
"aa_end": null,
"aa_length": 495,
"cds_start": 1072,
"cds_end": null,
"cds_length": 1488,
"cdna_start": 1258,
"cdna_end": null,
"cdna_length": 1943,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000883888.1"
},
{
"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": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PROC",
"gene_hgnc_id": 9451,
"hgvs_c": "c.1072G>A",
"hgvs_p": "p.Gly358Ser",
"transcript": "ENST00000883893.1",
"protein_id": "ENSP00000553952.1",
"transcript_support_level": null,
"aa_start": 358,
"aa_end": null,
"aa_length": 495,
"cds_start": 1072,
"cds_end": null,
"cds_length": 1488,
"cdna_start": 1309,
"cdna_end": null,
"cdna_length": 1793,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000883893.1"
},
{
"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": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PROC",
"gene_hgnc_id": 9451,
"hgvs_c": "c.1072G>A",
"hgvs_p": "p.Gly358Ser",
"transcript": "ENST00000883894.1",
"protein_id": "ENSP00000553953.1",
"transcript_support_level": null,
"aa_start": 358,
"aa_end": null,
"aa_length": 495,
"cds_start": 1072,
"cds_end": null,
"cds_length": 1488,
"cdna_start": 1313,
"cdna_end": null,
"cdna_length": 1797,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000883894.1"
},
{
"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": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PROC",
"gene_hgnc_id": 9451,
"hgvs_c": "c.1072G>A",
"hgvs_p": "p.Gly358Ser",
"transcript": "ENST00000883895.1",
"protein_id": "ENSP00000553954.1",
"transcript_support_level": null,
"aa_start": 358,
"aa_end": null,
"aa_length": 495,
"cds_start": 1072,
"cds_end": null,
"cds_length": 1488,
"cdna_start": 1254,
"cdna_end": null,
"cdna_length": 1738,
"mane_select": null,
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"verdict": "Uncertain_significance",
"transcript": "NM_001375607.1",
"gene_symbol": "PROC",
"hgnc_id": 9451,
"effects": [
"missense_variant"
],
"inheritance_mode": "SD,AD,AR",
"hgvs_c": "c.1156G>A",
"hgvs_p": "p.Gly386Ser"
},
{
"score": 0,
"benign_score": 1,
"pathogenic_score": 1,
"criteria": [
"PP5",
"BP4"
],
"verdict": "Uncertain_significance",
"transcript": "XR_007087228.1",
"gene_symbol": "LOC105373608",
"hgnc_id": null,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.1041-266C>T",
"hgvs_p": null
}
],
"clinvar_disease": " autosomal dominant,Thrombophilia due to protein C deficiency",
"clinvar_classification": "Likely pathogenic",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "LP:1",
"phenotype_combined": "Thrombophilia due to protein C deficiency, autosomal dominant",
"pathogenicity_classification_combined": "Likely pathogenic",
"custom_annotations": null
}
],
"message": null
}