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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: 11-117164013-T-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=117164013&ref=T&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "11",
"pos": 117164013,
"ref": "T",
"alt": "A",
"effect": "intron_variant",
"transcript": "NM_002572.4",
"consequences": [
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "PAFAH1B2",
"gene_hgnc_id": 8575,
"hgvs_c": "c.411+121T>A",
"hgvs_p": null,
"transcript": "NM_002572.4",
"protein_id": "NP_002563.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 229,
"cds_start": null,
"cds_end": null,
"cds_length": 690,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000527958.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_002572.4"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "PAFAH1B2",
"gene_hgnc_id": 8575,
"hgvs_c": "c.411+121T>A",
"hgvs_p": null,
"transcript": "ENST00000527958.6",
"protein_id": "ENSP00000435289.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 229,
"cds_start": null,
"cds_end": null,
"cds_length": 690,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_002572.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000527958.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "PAFAH1B2",
"gene_hgnc_id": 8575,
"hgvs_c": "c.411+121T>A",
"hgvs_p": null,
"transcript": "ENST00000530272.1",
"protein_id": "ENSP00000431365.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 202,
"cds_start": null,
"cds_end": null,
"cds_length": 609,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000530272.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "PAFAH1B2",
"gene_hgnc_id": 8575,
"hgvs_c": "c.249+121T>A",
"hgvs_p": null,
"transcript": "ENST00000304808.10",
"protein_id": "ENSP00000304006.6",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 175,
"cds_start": null,
"cds_end": null,
"cds_length": 528,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000304808.10"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "PAFAH1B2",
"gene_hgnc_id": 8575,
"hgvs_c": "c.411+121T>A",
"hgvs_p": null,
"transcript": "ENST00000529887.6",
"protein_id": "ENSP00000434951.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 155,
"cds_start": null,
"cds_end": null,
"cds_length": 468,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000529887.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "PAFAH1B2",
"gene_hgnc_id": 8575,
"hgvs_c": "c.417+121T>A",
"hgvs_p": null,
"transcript": "ENST00000948518.1",
"protein_id": "ENSP00000618577.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 231,
"cds_start": null,
"cds_end": null,
"cds_length": 696,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000948518.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "PAFAH1B2",
"gene_hgnc_id": 8575,
"hgvs_c": "c.411+121T>A",
"hgvs_p": null,
"transcript": "ENST00000903189.1",
"protein_id": "ENSP00000573248.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 229,
"cds_start": null,
"cds_end": null,
"cds_length": 690,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000903189.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 6,
"intron_rank_end": null,
"gene_symbol": "PAFAH1B2",
"gene_hgnc_id": 8575,
"hgvs_c": "c.411+121T>A",
"hgvs_p": null,
"transcript": "ENST00000903190.1",
"protein_id": "ENSP00000573249.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 229,
"cds_start": null,
"cds_end": null,
"cds_length": 690,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000903190.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "PAFAH1B2",
"gene_hgnc_id": 8575,
"hgvs_c": "c.411+121T>A",
"hgvs_p": null,
"transcript": "ENST00000903191.1",
"protein_id": "ENSP00000573250.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 229,
"cds_start": null,
"cds_end": null,
"cds_length": 690,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000903191.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "PAFAH1B2",
"gene_hgnc_id": 8575,
"hgvs_c": "c.411+121T>A",
"hgvs_p": null,
"transcript": "ENST00000903193.1",
"protein_id": "ENSP00000573252.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 229,
"cds_start": null,
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"cds_length": 690,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000903193.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 6,
"intron_rank_end": null,
"gene_symbol": "PAFAH1B2",
"gene_hgnc_id": 8575,
"hgvs_c": "c.411+121T>A",
"hgvs_p": null,
"transcript": "ENST00000903194.1",
"protein_id": "ENSP00000573253.1",
"transcript_support_level": null,
"aa_start": null,
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"aa_length": 229,
"cds_start": null,
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"cdna_start": null,
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"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000903194.1"
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 7,
"intron_rank": 6,
"intron_rank_end": null,
"gene_symbol": "PAFAH1B2",
"gene_hgnc_id": 8575,
"hgvs_c": "c.411+121T>A",
"hgvs_p": null,
"transcript": "ENST00000903195.1",
"protein_id": "ENSP00000573254.1",
"transcript_support_level": null,
"aa_start": null,
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"aa_length": 229,
"cds_start": null,
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"cdna_start": null,
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"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000903195.1"
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "PAFAH1B2",
"gene_hgnc_id": 8575,
"hgvs_c": "c.411+121T>A",
"hgvs_p": null,
"transcript": "ENST00000928783.1",
"protein_id": "ENSP00000598842.1",
"transcript_support_level": null,
"aa_start": null,
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"aa_length": 229,
"cds_start": null,
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"cdna_start": null,
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"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000928783.1"
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 7,
"intron_rank": 6,
"intron_rank_end": null,
"gene_symbol": "PAFAH1B2",
"gene_hgnc_id": 8575,
"hgvs_c": "c.411+121T>A",
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"transcript": "ENST00000928785.1",
"protein_id": "ENSP00000598844.1",
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"biotype": "protein_coding",
"feature": "ENST00000928785.1"
},
{
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"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 6,
"intron_rank_end": null,
"gene_symbol": "PAFAH1B2",
"gene_hgnc_id": 8575,
"hgvs_c": "c.411+121T>A",
"hgvs_p": null,
"transcript": "ENST00000928786.1",
"protein_id": "ENSP00000598845.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
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"cds_start": null,
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"cdna_start": null,
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"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000928786.1"
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 6,
"intron_rank_end": null,
"gene_symbol": "PAFAH1B2",
"gene_hgnc_id": 8575,
"hgvs_c": "c.411+121T>A",
"hgvs_p": null,
"transcript": "ENST00000928787.1",
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"mane_select": null,
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"biotype": "protein_coding",
"feature": "ENST00000928787.1"
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "PAFAH1B2",
"gene_hgnc_id": 8575,
"hgvs_c": "c.411+121T>A",
"hgvs_p": null,
"transcript": "ENST00000928788.1",
"protein_id": "ENSP00000598847.1",
"transcript_support_level": null,
"aa_start": null,
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"cds_start": null,
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"cdna_start": null,
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"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000928788.1"
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
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],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 6,
"intron_rank_end": null,
"gene_symbol": "PAFAH1B2",
"gene_hgnc_id": 8575,
"hgvs_c": "c.411+121T>A",
"hgvs_p": null,
"transcript": "ENST00000928789.1",
"protein_id": "ENSP00000598848.1",
"transcript_support_level": null,
"aa_start": null,
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"cds_start": null,
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},
{
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"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 7,
"intron_rank": 6,
"intron_rank_end": null,
"gene_symbol": "PAFAH1B2",
"gene_hgnc_id": 8575,
"hgvs_c": "c.411+121T>A",
"hgvs_p": null,
"transcript": "ENST00000948517.1",
"protein_id": "ENSP00000618576.1",
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},
{
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"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 6,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "PAFAH1B2",
"gene_hgnc_id": 8575,
"hgvs_c": "c.411+121T>A",
"hgvs_p": null,
"transcript": "ENST00000948519.1",
"protein_id": "ENSP00000618578.1",
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"feature": "ENST00000948519.1"
},
{
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"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 7,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "PAFAH1B2",
"gene_hgnc_id": 8575,
"hgvs_c": "c.411+121T>A",
"hgvs_p": null,
"transcript": "NM_001184746.2",
"protein_id": "NP_001171675.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 202,
"cds_start": null,
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"cds_length": 609,
"cdna_start": null,
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"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001184746.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "PAFAH1B2",
"gene_hgnc_id": 8575,
"hgvs_c": "c.321+121T>A",
"hgvs_p": null,
"transcript": "ENST00000928784.1",
"protein_id": "ENSP00000598843.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 199,
"cds_start": null,
"cds_end": null,
"cds_length": 600,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000928784.1"
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
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