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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: 11-70161378-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=70161378&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "11",
"pos": 70161378,
"ref": "C",
"alt": "G",
"effect": "intron_variant",
"transcript": "ENST00000355303.10",
"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": 26,
"intron_rank": 17,
"intron_rank_end": null,
"gene_symbol": "ANO1",
"gene_hgnc_id": 21625,
"hgvs_c": "c.1780+16C>G",
"hgvs_p": null,
"transcript": "NM_018043.7",
"protein_id": "NP_060513.5",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 986,
"cds_start": -4,
"cds_end": null,
"cds_length": 2961,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4777,
"mane_select": "ENST00000355303.10",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 26,
"intron_rank": 17,
"intron_rank_end": null,
"gene_symbol": "ANO1",
"gene_hgnc_id": 21625,
"hgvs_c": "c.1780+16C>G",
"hgvs_p": null,
"transcript": "ENST00000355303.10",
"protein_id": "ENSP00000347454.5",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 986,
"cds_start": -4,
"cds_end": null,
"cds_length": 2961,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4777,
"mane_select": "NM_018043.7",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 28,
"intron_rank": 19,
"intron_rank_end": null,
"gene_symbol": "ANO1",
"gene_hgnc_id": 21625,
"hgvs_c": "c.1969+16C>G",
"hgvs_p": null,
"transcript": "ENST00000531349.6",
"protein_id": "ENSP00000432843.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1049,
"cds_start": -4,
"cds_end": null,
"cds_length": 3150,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4878,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 28,
"intron_rank": 19,
"intron_rank_end": null,
"gene_symbol": "ANO1",
"gene_hgnc_id": 21625,
"hgvs_c": "c.1969+16C>G",
"hgvs_p": null,
"transcript": "NM_001378092.1",
"protein_id": "NP_001365021.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1049,
"cds_start": -4,
"cds_end": null,
"cds_length": 3150,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4878,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 26,
"intron_rank": 17,
"intron_rank_end": null,
"gene_symbol": "ANO1",
"gene_hgnc_id": 21625,
"hgvs_c": "c.1768+16C>G",
"hgvs_p": null,
"transcript": "NM_001378093.1",
"protein_id": "NP_001365022.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 982,
"cds_start": -4,
"cds_end": null,
"cds_length": 2949,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4613,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 25,
"intron_rank": 16,
"intron_rank_end": null,
"gene_symbol": "ANO1",
"gene_hgnc_id": 21625,
"hgvs_c": "c.1768+16C>G",
"hgvs_p": null,
"transcript": "NM_001378094.2",
"protein_id": "NP_001365023.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 982,
"cds_start": -4,
"cds_end": null,
"cds_length": 2949,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4765,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 26,
"intron_rank": 17,
"intron_rank_end": null,
"gene_symbol": "ANO1",
"gene_hgnc_id": 21625,
"hgvs_c": "c.1768+16C>G",
"hgvs_p": null,
"transcript": "NM_001378095.2",
"protein_id": "NP_001365024.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 982,
"cds_start": -4,
"cds_end": null,
"cds_length": 2949,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4765,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 24,
"intron_rank": 15,
"intron_rank_end": null,
"gene_symbol": "ANO1",
"gene_hgnc_id": 21625,
"hgvs_c": "c.1690+16C>G",
"hgvs_p": null,
"transcript": "NM_001378096.2",
"protein_id": "NP_001365025.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 956,
"cds_start": -4,
"cds_end": null,
"cds_length": 2871,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4687,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 24,
"intron_rank": 15,
"intron_rank_end": null,
"gene_symbol": "ANO1",
"gene_hgnc_id": 21625,
"hgvs_c": "c.1603+16C>G",
"hgvs_p": null,
"transcript": "NM_001378097.2",
"protein_id": "NP_001365026.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 927,
"cds_start": -4,
"cds_end": null,
"cds_length": 2784,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4600,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 25,
"intron_rank": 15,
"intron_rank_end": null,
"gene_symbol": "ANO1",
"gene_hgnc_id": 21625,
"hgvs_c": "c.1342+16C>G",
"hgvs_p": null,
"transcript": "ENST00000530676.5",
"protein_id": "ENSP00000435797.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 840,
"cds_start": -4,
"cds_end": null,
"cds_length": 2523,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3289,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 17,
"intron_rank": 15,
"intron_rank_end": null,
"gene_symbol": "ANO1",
"gene_hgnc_id": 21625,
"hgvs_c": "c.1606+16C>G",
"hgvs_p": null,
"transcript": "ENST00000316296.9",
"protein_id": "ENSP00000319477.5",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 642,
"cds_start": -4,
"cds_end": null,
"cds_length": 1929,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2118,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
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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": "ANO1",
"gene_hgnc_id": 21625,
"hgvs_c": "c.433+16C>G",
"hgvs_p": null,
"transcript": "ENST00000531300.1",
"protein_id": "ENSP00000435868.1",
"transcript_support_level": 4,
"aa_start": null,
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"aa_length": 150,
"cds_start": -4,
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"cds_length": 454,
"cdna_start": null,
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"cdna_length": 577,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": 11,
"intron_rank_end": null,
"gene_symbol": "ANO1",
"gene_hgnc_id": 21625,
"hgvs_c": "n.1123+16C>G",
"hgvs_p": null,
"transcript": "ENST00000689710.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
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"aa_length": null,
"cds_start": -4,
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"cdna_start": null,
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"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 25,
"intron_rank": 15,
"intron_rank_end": null,
"gene_symbol": "ANO1",
"gene_hgnc_id": 21625,
"hgvs_c": "n.1835+16C>G",
"hgvs_p": null,
"transcript": "NR_030691.2",
"protein_id": null,
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"aa_start": null,
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"aa_length": null,
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},
{
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"strand": true,
"consequences": [
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],
"exon_rank": null,
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"intron_rank": 17,
"intron_rank_end": null,
"gene_symbol": "ANO1",
"gene_hgnc_id": 21625,
"hgvs_c": "c.1879+16C>G",
"hgvs_p": null,
"transcript": "XM_047427181.1",
"protein_id": "XP_047283137.1",
"transcript_support_level": null,
"aa_start": null,
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"aa_length": 1019,
"cds_start": -4,
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"cdna_start": null,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
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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": 28,
"intron_rank": 19,
"intron_rank_end": null,
"gene_symbol": "ANO1",
"gene_hgnc_id": 21625,
"hgvs_c": "c.1846+16C>G",
"hgvs_p": null,
"transcript": "XM_047427182.1",
"protein_id": "XP_047283138.1",
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},
{
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],
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"intron_rank": 19,
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"gene_symbol": "ANO1",
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"hgvs_c": "c.1846+16C>G",
"hgvs_p": null,
"transcript": "XM_047427183.1",
"protein_id": "XP_047283139.1",
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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": 27,
"intron_rank": 18,
"intron_rank_end": null,
"gene_symbol": "ANO1",
"gene_hgnc_id": 21625,
"hgvs_c": "c.1843+16C>G",
"hgvs_p": null,
"transcript": "XM_011545123.3",
"protein_id": "XP_011543425.1",
"transcript_support_level": null,
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},
{
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"protein_coding": true,
"strand": true,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 25,
"intron_rank": 16,
"intron_rank_end": null,
"gene_symbol": "ANO1",
"gene_hgnc_id": 21625,
"hgvs_c": "c.1837+16C>G",
"hgvs_p": null,
"transcript": "XM_047427185.1",
"protein_id": "XP_047283141.1",
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},
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],
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"gene_symbol": "ANO1",
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"hgvs_c": "c.1834+16C>G",
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"transcript": "XM_011545124.3",
"protein_id": "XP_011543426.1",
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},
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"strand": true,
"consequences": [
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],
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"intron_rank": 16,
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"gene_symbol": "ANO1",
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"hgvs_c": "c.1813+16C>G",
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},
{
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"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": 18,
"intron_rank_end": null,
"gene_symbol": "ANO1",
"gene_hgnc_id": 21625,
"hgvs_c": "c.1780+16C>G",
"hgvs_p": null,
"transcript": "XM_047427186.1",
"protein_id": "XP_047283142.1",
"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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"cdna_length": 4625,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": 18,
"intron_rank_end": null,
"gene_symbol": "ANO1",
"gene_hgnc_id": 21625,
"hgvs_c": "c.1762+16C>G",
"hgvs_p": null,
"transcript": "XM_006718602.3",
"protein_id": "XP_006718665.1",
"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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"mane_select": null,
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}
],
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}