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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: X-19082468-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=19082468&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "X",
"pos": 19082468,
"ref": "G",
"alt": "C",
"effect": "intron_variant",
"transcript": "ENST00000379869.8",
"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": 29,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ADGRG2",
"gene_hgnc_id": 4516,
"hgvs_c": "c.-2+234C>G",
"hgvs_p": null,
"transcript": "NM_001079858.3",
"protein_id": "NP_001073327.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1017,
"cds_start": -4,
"cds_end": null,
"cds_length": 3054,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4684,
"mane_select": "ENST00000379869.8",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 29,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ADGRG2",
"gene_hgnc_id": 4516,
"hgvs_c": "c.-2+234C>G",
"hgvs_p": null,
"transcript": "ENST00000379869.8",
"protein_id": "ENSP00000369198.3",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1017,
"cds_start": -4,
"cds_end": null,
"cds_length": 3054,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4684,
"mane_select": "NM_001079858.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 29,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ADGRG2",
"gene_hgnc_id": 4516,
"hgvs_c": "c.-2+234C>G",
"hgvs_p": null,
"transcript": "ENST00000357991.7",
"protein_id": "ENSP00000350680.3",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1014,
"cds_start": -4,
"cds_end": null,
"cds_length": 3045,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4661,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 28,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ADGRG2",
"gene_hgnc_id": 4516,
"hgvs_c": "c.-2+234C>G",
"hgvs_p": null,
"transcript": "ENST00000356606.8",
"protein_id": "ENSP00000349015.4",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1003,
"cds_start": -4,
"cds_end": null,
"cds_length": 3012,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4630,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 28,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ADGRG2",
"gene_hgnc_id": 4516,
"hgvs_c": "c.-2+234C>G",
"hgvs_p": null,
"transcript": "ENST00000379878.7",
"protein_id": "ENSP00000369207.3",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1001,
"cds_start": -4,
"cds_end": null,
"cds_length": 3006,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4803,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 27,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ADGRG2",
"gene_hgnc_id": 4516,
"hgvs_c": "c.-2+234C>G",
"hgvs_p": null,
"transcript": "ENST00000360279.8",
"protein_id": "ENSP00000353421.4",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 995,
"cds_start": -4,
"cds_end": null,
"cds_length": 2988,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4702,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 27,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ADGRG2",
"gene_hgnc_id": 4516,
"hgvs_c": "c.-2+234C>G",
"hgvs_p": null,
"transcript": "ENST00000379876.5",
"protein_id": "ENSP00000369205.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 993,
"cds_start": -4,
"cds_end": null,
"cds_length": 2982,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4779,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 27,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ADGRG2",
"gene_hgnc_id": 4516,
"hgvs_c": "c.-2+234C>G",
"hgvs_p": null,
"transcript": "ENST00000357544.7",
"protein_id": "ENSP00000350152.3",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 987,
"cds_start": -4,
"cds_end": null,
"cds_length": 2964,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4678,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 28,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ADGRG2",
"gene_hgnc_id": 4516,
"hgvs_c": "c.-2+234C>G",
"hgvs_p": null,
"transcript": "ENST00000379873.6",
"protein_id": "ENSP00000369202.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 966,
"cds_start": -4,
"cds_end": null,
"cds_length": 2901,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4698,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ADGRG2",
"gene_hgnc_id": 4516,
"hgvs_c": "c.-2+234C>G",
"hgvs_p": null,
"transcript": "NM_005756.4",
"protein_id": "NP_005747.2",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1014,
"cds_start": -4,
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"cds_length": 3045,
"cdna_start": null,
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"cdna_length": 4675,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ADGRG2",
"gene_hgnc_id": 4516,
"hgvs_c": "c.-2+234C>G",
"hgvs_p": null,
"transcript": "NM_001079859.3",
"protein_id": "NP_001073328.1",
"transcript_support_level": null,
"aa_start": null,
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"cds_start": -4,
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"cdna_start": null,
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"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 28,
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"gene_symbol": "ADGRG2",
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"hgvs_c": "c.-2+234C>G",
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"transcript": "NM_001184833.2",
"protein_id": "NP_001171762.1",
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"feature": null
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 27,
"intron_rank": 2,
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"gene_symbol": "ADGRG2",
"gene_hgnc_id": 4516,
"hgvs_c": "c.-2+234C>G",
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"transcript": "NM_001079860.3",
"protein_id": "NP_001073329.1",
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},
{
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"strand": false,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 27,
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"gene_symbol": "ADGRG2",
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"hgvs_c": "c.-2+234C>G",
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"transcript": "NM_001184836.2",
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},
{
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],
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"gene_symbol": "ADGRG2",
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"hgvs_c": "c.-2+234C>G",
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"transcript": "NM_001184837.2",
"protein_id": "NP_001171766.1",
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"mane_select": null,
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},
{
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"strand": false,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 26,
"intron_rank": 2,
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"gene_symbol": "ADGRG2",
"gene_hgnc_id": 4516,
"hgvs_c": "c.-2+234C>G",
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"transcript": "NM_001184835.2",
"protein_id": "NP_001171764.1",
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},
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],
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"gene_symbol": "ADGRG2",
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"hgvs_c": "c.-2+234C>G",
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"transcript": "NM_001184834.2",
"protein_id": "NP_001171763.1",
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},
{
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"strand": false,
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],
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"exon_count": 24,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ADGRG2",
"gene_hgnc_id": 4516,
"hgvs_c": "c.-2+234C>G",
"hgvs_p": null,
"transcript": "ENST00000340581.3",
"protein_id": "ENSP00000344972.3",
"transcript_support_level": 2,
"aa_start": null,
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},
{
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"strand": false,
"consequences": [
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],
"exon_rank": null,
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"intron_rank": 2,
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"gene_symbol": "ADGRG2",
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"hgvs_c": "c.-2+234C>G",
"hgvs_p": null,
"transcript": "ENST00000354791.7",
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},
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],
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"gene_symbol": "ADGRG2",
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"hgvs_c": "c.113+234C>G",
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},
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],
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"gene_symbol": "ADGRG2",
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},
{
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"strand": false,
"consequences": [
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],
"exon_rank": null,
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"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ADGRG2",
"gene_hgnc_id": 4516,
"hgvs_c": "c.-2+234C>G",
"hgvs_p": null,
"transcript": "XM_011545434.2",
"protein_id": "XP_011543736.1",
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"aa_start": null,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 29,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ADGRG2",
"gene_hgnc_id": 4516,
"hgvs_c": "c.-2+234C>G",
"hgvs_p": null,
"transcript": "XM_011545435.3",
"protein_id": "XP_011543737.1",
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}
],
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}