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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: 2-37201874-G-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=37201874&ref=G&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 37201874,
"ref": "G",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_005760.3",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEBPZ",
"gene_hgnc_id": 24218,
"hgvs_c": "c.3055C>A",
"hgvs_p": "p.Arg1019Ser",
"transcript": "NM_005760.3",
"protein_id": "NP_005751.2",
"transcript_support_level": null,
"aa_start": 1019,
"aa_end": null,
"aa_length": 1054,
"cds_start": 3055,
"cds_end": null,
"cds_length": 3165,
"cdna_start": 3084,
"cdna_end": null,
"cdna_length": 3346,
"mane_select": "ENST00000234170.10",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_005760.3"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEBPZ",
"gene_hgnc_id": 24218,
"hgvs_c": "c.3055C>A",
"hgvs_p": "p.Arg1019Ser",
"transcript": "ENST00000234170.10",
"protein_id": "ENSP00000234170.5",
"transcript_support_level": 1,
"aa_start": 1019,
"aa_end": null,
"aa_length": 1054,
"cds_start": 3055,
"cds_end": null,
"cds_length": 3165,
"cdna_start": 3084,
"cdna_end": null,
"cdna_length": 3346,
"mane_select": "NM_005760.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000234170.10"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEBPZOS",
"gene_hgnc_id": 49288,
"hgvs_c": "c.*14G>T",
"hgvs_p": null,
"transcript": "NM_001322374.2",
"protein_id": "NP_001309303.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 80,
"cds_start": null,
"cds_end": null,
"cds_length": 243,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3152,
"mane_select": "ENST00000402297.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001322374.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEBPZOS",
"gene_hgnc_id": 49288,
"hgvs_c": "c.*14G>T",
"hgvs_p": null,
"transcript": "ENST00000402297.6",
"protein_id": "ENSP00000384331.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 80,
"cds_start": null,
"cds_end": null,
"cds_length": 243,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3152,
"mane_select": "NM_001322374.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000402297.6"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEBPZ",
"gene_hgnc_id": 24218,
"hgvs_c": "c.3073C>A",
"hgvs_p": "p.Arg1025Ser",
"transcript": "ENST00000898579.1",
"protein_id": "ENSP00000568638.1",
"transcript_support_level": null,
"aa_start": 1025,
"aa_end": null,
"aa_length": 1060,
"cds_start": 3073,
"cds_end": null,
"cds_length": 3183,
"cdna_start": 3095,
"cdna_end": null,
"cdna_length": 3248,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898579.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEBPZ",
"gene_hgnc_id": 24218,
"hgvs_c": "c.3052C>A",
"hgvs_p": "p.Arg1018Ser",
"transcript": "ENST00000938546.1",
"protein_id": "ENSP00000608605.1",
"transcript_support_level": null,
"aa_start": 1018,
"aa_end": null,
"aa_length": 1053,
"cds_start": 3052,
"cds_end": null,
"cds_length": 3162,
"cdna_start": 3081,
"cdna_end": null,
"cdna_length": 3385,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000938546.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEBPZ",
"gene_hgnc_id": 24218,
"hgvs_c": "c.2944C>A",
"hgvs_p": "p.Arg982Ser",
"transcript": "ENST00000938548.1",
"protein_id": "ENSP00000608607.1",
"transcript_support_level": null,
"aa_start": 982,
"aa_end": null,
"aa_length": 1017,
"cds_start": 2944,
"cds_end": null,
"cds_length": 3054,
"cdna_start": 2972,
"cdna_end": null,
"cdna_length": 3122,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000938548.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEBPZ",
"gene_hgnc_id": 24218,
"hgvs_c": "c.2914C>A",
"hgvs_p": "p.Arg972Ser",
"transcript": "ENST00000938547.1",
"protein_id": "ENSP00000608606.1",
"transcript_support_level": null,
"aa_start": 972,
"aa_end": null,
"aa_length": 1007,
"cds_start": 2914,
"cds_end": null,
"cds_length": 3024,
"cdna_start": 2948,
"cdna_end": null,
"cdna_length": 3207,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000938547.1"
},
{
"aa_ref": "R",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEBPZ",
"gene_hgnc_id": 24218,
"hgvs_c": "c.2740C>A",
"hgvs_p": "p.Arg914Ser",
"transcript": "ENST00000898578.1",
"protein_id": "ENSP00000568637.1",
"transcript_support_level": null,
"aa_start": 914,
"aa_end": null,
"aa_length": 949,
"cds_start": 2740,
"cds_end": null,
"cds_length": 2850,
"cdna_start": 2769,
"cdna_end": null,
"cdna_length": 2922,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898578.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEBPZOS",
"gene_hgnc_id": 49288,
"hgvs_c": "c.*14G>T",
"hgvs_p": null,
"transcript": "NM_001322373.2",
"protein_id": "NP_001309302.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 80,
"cds_start": null,
"cds_end": null,
"cds_length": 243,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3331,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001322373.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEBPZOS",
"gene_hgnc_id": 49288,
"hgvs_c": "c.*10G>T",
"hgvs_p": null,
"transcript": "NM_001322376.2",
"protein_id": "NP_001309305.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 80,
"cds_start": null,
"cds_end": null,
"cds_length": 243,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3148,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001322376.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEBPZOS",
"gene_hgnc_id": 49288,
"hgvs_c": "c.*14G>T",
"hgvs_p": null,
"transcript": "ENST00000397226.2",
"protein_id": "ENSP00000380403.2",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 80,
"cds_start": null,
"cds_end": null,
"cds_length": 243,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1499,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000397226.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEBPZOS",
"gene_hgnc_id": 49288,
"hgvs_c": "c.*14G>T",
"hgvs_p": null,
"transcript": "ENST00000898770.1",
"protein_id": "ENSP00000568829.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 80,
"cds_start": null,
"cds_end": null,
"cds_length": 243,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3249,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898770.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEBPZOS",
"gene_hgnc_id": 49288,
"hgvs_c": "c.*14G>T",
"hgvs_p": null,
"transcript": "ENST00000898774.1",
"protein_id": "ENSP00000568833.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 80,
"cds_start": null,
"cds_end": null,
"cds_length": 243,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1376,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898774.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEBPZOS",
"gene_hgnc_id": 49288,
"hgvs_c": "c.*14G>T",
"hgvs_p": null,
"transcript": "ENST00000898775.1",
"protein_id": "ENSP00000568834.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 80,
"cds_start": null,
"cds_end": null,
"cds_length": 243,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1360,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898775.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEBPZOS",
"gene_hgnc_id": 49288,
"hgvs_c": "c.*10G>T",
"hgvs_p": null,
"transcript": "ENST00000898776.1",
"protein_id": "ENSP00000568835.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 80,
"cds_start": null,
"cds_end": null,
"cds_length": 243,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1077,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898776.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEBPZOS",
"gene_hgnc_id": 49288,
"hgvs_c": "c.*14G>T",
"hgvs_p": null,
"transcript": "ENST00000898777.1",
"protein_id": "ENSP00000568836.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 80,
"cds_start": null,
"cds_end": null,
"cds_length": 243,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1352,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898777.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEBPZOS",
"gene_hgnc_id": 49288,
"hgvs_c": "c.*150G>T",
"hgvs_p": null,
"transcript": "ENST00000898778.1",
"protein_id": "ENSP00000568837.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 80,
"cds_start": null,
"cds_end": null,
"cds_length": 243,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1193,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898778.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEBPZOS",
"gene_hgnc_id": 49288,
"hgvs_c": "c.*14G>T",
"hgvs_p": null,
"transcript": "ENST00000898779.1",
"protein_id": "ENSP00000568838.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 80,
"cds_start": null,
"cds_end": null,
"cds_length": 243,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1416,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898779.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEBPZOS",
"gene_hgnc_id": 49288,
"hgvs_c": "c.*14G>T",
"hgvs_p": null,
"transcript": "ENST00000898780.1",
"protein_id": "ENSP00000568839.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 80,
"cds_start": null,
"cds_end": null,
"cds_length": 243,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1137,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898780.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEBPZOS",
"gene_hgnc_id": 49288,
"hgvs_c": "c.*14G>T",
"hgvs_p": null,
"transcript": "ENST00000938662.1",
"protein_id": "ENSP00000608721.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 80,
"cds_start": null,
"cds_end": null,
"cds_length": 243,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3550,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000938662.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEBPZOS",
"gene_hgnc_id": 49288,
"hgvs_c": "c.*14G>T",
"hgvs_p": null,
"transcript": "ENST00000938664.1",
"protein_id": "ENSP00000608723.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 80,
"cds_start": null,
"cds_end": null,
"cds_length": 243,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3309,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000938664.1"
},
{
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{
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],
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"clinvar_submissions_summary": "US:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Uncertain significance",
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}
],
"message": null
}