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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: 11-72959855-T-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=72959855&ref=T&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "11",
"pos": 72959855,
"ref": "T",
"alt": "G",
"effect": "intron_variant",
"transcript": "NM_014824.3",
"consequences": [
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "FCHSD2",
"gene_hgnc_id": 29114,
"hgvs_c": "c.705+24233A>C",
"hgvs_p": null,
"transcript": "NM_014824.3",
"protein_id": "NP_055639.2",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 740,
"cds_start": null,
"cds_end": null,
"cds_length": 2223,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000409418.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_014824.3"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "FCHSD2",
"gene_hgnc_id": 29114,
"hgvs_c": "c.705+24233A>C",
"hgvs_p": null,
"transcript": "ENST00000409418.9",
"protein_id": "ENSP00000386722.4",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 740,
"cds_start": null,
"cds_end": null,
"cds_length": 2223,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_014824.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000409418.9"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": 7,
"intron_rank_end": null,
"gene_symbol": "FCHSD2",
"gene_hgnc_id": 29114,
"hgvs_c": "c.537+24233A>C",
"hgvs_p": null,
"transcript": "ENST00000311172.11",
"protein_id": "ENSP00000308978.7",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 684,
"cds_start": null,
"cds_end": null,
"cds_length": 2055,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000311172.11"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "FCHSD2",
"gene_hgnc_id": 29114,
"hgvs_c": "c.537+24233A>C",
"hgvs_p": null,
"transcript": "ENST00000409853.5",
"protein_id": "ENSP00000386314.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 515,
"cds_start": null,
"cds_end": null,
"cds_length": 1548,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000409853.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "FCHSD2",
"gene_hgnc_id": 29114,
"hgvs_c": "c.705+24233A>C",
"hgvs_p": null,
"transcript": "ENST00000409314.5",
"protein_id": "ENSP00000386987.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 764,
"cds_start": null,
"cds_end": null,
"cds_length": 2295,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000409314.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "FCHSD2",
"gene_hgnc_id": 29114,
"hgvs_c": "c.705+24233A>C",
"hgvs_p": null,
"transcript": "ENST00000891583.1",
"protein_id": "ENSP00000561642.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 760,
"cds_start": null,
"cds_end": null,
"cds_length": 2283,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000891583.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": 9,
"intron_rank_end": null,
"gene_symbol": "FCHSD2",
"gene_hgnc_id": 29114,
"hgvs_c": "c.750+4138A>C",
"hgvs_p": null,
"transcript": "ENST00000891582.1",
"protein_id": "ENSP00000561641.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 755,
"cds_start": null,
"cds_end": null,
"cds_length": 2268,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000891582.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "FCHSD2",
"gene_hgnc_id": 29114,
"hgvs_c": "c.705+24233A>C",
"hgvs_p": null,
"transcript": "ENST00000891581.1",
"protein_id": "ENSP00000561640.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 748,
"cds_start": null,
"cds_end": null,
"cds_length": 2247,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000891581.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "FCHSD2",
"gene_hgnc_id": 29114,
"hgvs_c": "c.705+24233A>C",
"hgvs_p": null,
"transcript": "ENST00000891572.1",
"protein_id": "ENSP00000561631.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 738,
"cds_start": null,
"cds_end": null,
"cds_length": 2217,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000891572.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "FCHSD2",
"gene_hgnc_id": 29114,
"hgvs_c": "c.705+24233A>C",
"hgvs_p": null,
"transcript": "ENST00000891579.1",
"protein_id": "ENSP00000561638.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 716,
"cds_start": null,
"cds_end": null,
"cds_length": 2151,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000891579.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "FCHSD2",
"gene_hgnc_id": 29114,
"hgvs_c": "c.705+24233A>C",
"hgvs_p": null,
"transcript": "ENST00000891576.1",
"protein_id": "ENSP00000561635.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 708,
"cds_start": null,
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"cds_length": 2127,
"cdna_start": null,
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"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000891576.1"
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 20,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "FCHSD2",
"gene_hgnc_id": 29114,
"hgvs_c": "c.606+24233A>C",
"hgvs_p": null,
"transcript": "ENST00000891577.1",
"protein_id": "ENSP00000561636.1",
"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,
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"biotype": "protein_coding",
"feature": "ENST00000891577.1"
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "FCHSD2",
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"hgvs_c": "c.705+24233A>C",
"hgvs_p": null,
"transcript": "ENST00000891580.1",
"protein_id": "ENSP00000561639.1",
"transcript_support_level": null,
"aa_start": null,
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"aa_length": 705,
"cds_start": null,
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"cdna_start": null,
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"mane_select": null,
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"biotype": "protein_coding",
"feature": "ENST00000891580.1"
},
{
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"strand": false,
"consequences": [
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],
"exon_rank": null,
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"gene_symbol": "FCHSD2",
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"hgvs_c": "c.705+24233A>C",
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"feature": "ENST00000960170.1"
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 19,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "FCHSD2",
"gene_hgnc_id": 29114,
"hgvs_c": "c.705+24233A>C",
"hgvs_p": null,
"transcript": "ENST00000891575.1",
"protein_id": "ENSP00000561634.1",
"transcript_support_level": null,
"aa_start": null,
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"mane_plus": null,
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"feature": "ENST00000891575.1"
},
{
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"strand": false,
"consequences": [
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],
"exon_rank": null,
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"intron_rank": 8,
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"gene_symbol": "FCHSD2",
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"hgvs_c": "c.705+24233A>C",
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"transcript": "ENST00000960169.1",
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"biotype": "protein_coding",
"feature": "ENST00000960169.1"
},
{
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"canonical": false,
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"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 19,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "FCHSD2",
"gene_hgnc_id": 29114,
"hgvs_c": "c.705+24233A>C",
"hgvs_p": null,
"transcript": "ENST00000891573.1",
"protein_id": "ENSP00000561632.1",
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"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000891573.1"
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "FCHSD2",
"gene_hgnc_id": 29114,
"hgvs_c": "c.705+24233A>C",
"hgvs_p": null,
"transcript": "ENST00000891574.1",
"protein_id": "ENSP00000561633.1",
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},
{
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"strand": false,
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],
"exon_rank": null,
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"exon_count": 18,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "FCHSD2",
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"hgvs_c": "c.705+24233A>C",
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},
{
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"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"intron_rank": 7,
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"gene_symbol": "FCHSD2",
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"hgvs_c": "c.225+24233A>C",
"hgvs_p": null,
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},
{
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"consequences": [
"intron_variant"
],
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"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "FCHSD2",
"gene_hgnc_id": 29114,
"hgvs_c": "c.166-37905A>C",
"hgvs_p": null,
"transcript": "ENST00000891578.1",
"protein_id": "ENSP00000561637.1",
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"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": "ENST00000891578.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "FCHSD2",
"gene_hgnc_id": 29114,
"hgvs_c": "c.642+24233A>C",
"hgvs_p": null,
"transcript": "XM_011545409.2",
"protein_id": "XP_011543711.1",
"transcript_support_level": null,
"aa_start": null,
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"aa_length": 719,
"cds_start": null,
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"cdna_start": null,
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"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011545409.2"
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
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],
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{
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{
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"splice_prediction_selected": "Benign",
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"phylop100way_prediction": "Benign",
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{
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"verdict": "Benign",
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],
"clinvar_disease": "",
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"clinvar_review_status": "",
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"custom_annotations": null
}
],
"message": null
}