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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: 7-14565273-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=14565273&ref=A&alt=G&genome=hg38&allGenes=true"
API Response
json
{
"variants": [
{
"chr": "7",
"pos": 14565273,
"ref": "A",
"alt": "G",
"effect": "intron_variant",
"transcript": "ENST00000402815.6",
"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": 26,
"intron_rank": 20,
"intron_rank_end": null,
"gene_symbol": "DGKB",
"gene_hgnc_id": 2850,
"hgvs_c": "c.1770+8939T>C",
"hgvs_p": null,
"transcript": "NM_001350709.2",
"protein_id": "NP_001337638.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 803,
"cds_start": -4,
"cds_end": null,
"cds_length": 2412,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6841,
"mane_select": "ENST00000402815.6",
"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": 26,
"intron_rank": 20,
"intron_rank_end": null,
"gene_symbol": "DGKB",
"gene_hgnc_id": 2850,
"hgvs_c": "c.1770+8939T>C",
"hgvs_p": null,
"transcript": "ENST00000402815.6",
"protein_id": "ENSP00000384909.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 803,
"cds_start": -4,
"cds_end": null,
"cds_length": 2412,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6841,
"mane_select": "NM_001350709.2",
"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": 24,
"intron_rank": 19,
"intron_rank_end": null,
"gene_symbol": "DGKB",
"gene_hgnc_id": 2850,
"hgvs_c": "c.1773+8939T>C",
"hgvs_p": null,
"transcript": "ENST00000406247.7",
"protein_id": "ENSP00000386066.3",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 773,
"cds_start": -4,
"cds_end": null,
"cds_length": 2322,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3257,
"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": 26,
"intron_rank": 20,
"intron_rank_end": null,
"gene_symbol": "DGKB",
"gene_hgnc_id": 2850,
"hgvs_c": "c.1773+8939T>C",
"hgvs_p": null,
"transcript": "NM_001350705.1",
"protein_id": "NP_001337634.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 804,
"cds_start": -4,
"cds_end": null,
"cds_length": 2415,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7212,
"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": 26,
"intron_rank": 20,
"intron_rank_end": null,
"gene_symbol": "DGKB",
"gene_hgnc_id": 2850,
"hgvs_c": "c.1773+8939T>C",
"hgvs_p": null,
"transcript": "NM_001350706.2",
"protein_id": "NP_001337635.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 804,
"cds_start": -4,
"cds_end": null,
"cds_length": 2415,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6844,
"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": 25,
"intron_rank": 19,
"intron_rank_end": null,
"gene_symbol": "DGKB",
"gene_hgnc_id": 2850,
"hgvs_c": "c.1773+8939T>C",
"hgvs_p": null,
"transcript": "ENST00000399322.7",
"protein_id": "ENSP00000382260.3",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 804,
"cds_start": -4,
"cds_end": null,
"cds_length": 2415,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6684,
"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": 26,
"intron_rank": 20,
"intron_rank_end": null,
"gene_symbol": "DGKB",
"gene_hgnc_id": 2850,
"hgvs_c": "c.1773+8939T>C",
"hgvs_p": null,
"transcript": "ENST00000403951.6",
"protein_id": "ENSP00000385780.2",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 804,
"cds_start": -4,
"cds_end": null,
"cds_length": 2415,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6917,
"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": 26,
"intron_rank": 20,
"intron_rank_end": null,
"gene_symbol": "DGKB",
"gene_hgnc_id": 2850,
"hgvs_c": "c.1770+8939T>C",
"hgvs_p": null,
"transcript": "NM_001350707.2",
"protein_id": "NP_001337636.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 803,
"cds_start": -4,
"cds_end": null,
"cds_length": 2412,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6844,
"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": 26,
"intron_rank": 20,
"intron_rank_end": null,
"gene_symbol": "DGKB",
"gene_hgnc_id": 2850,
"hgvs_c": "c.1770+8939T>C",
"hgvs_p": null,
"transcript": "NM_001350708.1",
"protein_id": "NP_001337637.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 803,
"cds_start": -4,
"cds_end": null,
"cds_length": 2412,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7209,
"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": 25,
"intron_rank": 19,
"intron_rank_end": null,
"gene_symbol": "DGKB",
"gene_hgnc_id": 2850,
"hgvs_c": "c.1752+8939T>C",
"hgvs_p": null,
"transcript": "NM_001350715.1",
"protein_id": "NP_001337644.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 797,
"cds_start": -4,
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"cds_length": 2394,
"cdna_start": null,
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"cdna_length": 7191,
"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": 25,
"intron_rank": 19,
"intron_rank_end": null,
"gene_symbol": "DGKB",
"gene_hgnc_id": 2850,
"hgvs_c": "c.1752+8939T>C",
"hgvs_p": null,
"transcript": "NM_001350716.2",
"protein_id": "NP_001337645.1",
"transcript_support_level": null,
"aa_start": null,
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"aa_length": 797,
"cds_start": -4,
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"cdna_start": null,
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"biotype": null,
"feature": null
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": null,
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"gene_symbol": "DGKB",
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"hgvs_c": "c.1749+8939T>C",
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"transcript": "NM_001350711.2",
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"cds_start": -4,
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"cdna_start": null,
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"feature": null
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"gene_symbol": "DGKB",
"gene_hgnc_id": 2850,
"hgvs_c": "c.1749+8939T>C",
"hgvs_p": null,
"transcript": "NM_001350712.1",
"protein_id": "NP_001337641.1",
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],
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"exon_count": 25,
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"gene_symbol": "DGKB",
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"hgvs_c": "c.1749+8939T>C",
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"transcript": "NM_001350714.2",
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},
{
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],
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"gene_symbol": "DGKB",
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"hgvs_c": "c.1749+8939T>C",
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"transcript": "ENST00000407950.5",
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},
{
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"strand": false,
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],
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"gene_symbol": "DGKB",
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"hgvs_c": "c.1737+8939T>C",
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"transcript": "NM_001350717.2",
"protein_id": "NP_001337646.1",
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{
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"gene_symbol": "DGKB",
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"hgvs_c": "c.1737+8939T>C",
"hgvs_p": null,
"transcript": "NM_001350718.1",
"protein_id": "NP_001337647.1",
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},
{
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],
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"gene_symbol": "DGKB",
"gene_hgnc_id": 2850,
"hgvs_c": "c.1737+8939T>C",
"hgvs_p": null,
"transcript": "NM_001350719.2",
"protein_id": "NP_001337648.1",
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{
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"gene_symbol": "DGKB",
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"hgvs_c": "c.1716+8939T>C",
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"protein_id": "NP_001337649.1",
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],
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"gene_symbol": "DGKB",
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"transcript": "NM_001350721.2",
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],
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"gene_symbol": "DGKB",
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"hgvs_c": "c.1773+8939T>C",
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},
{
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"strand": false,
"consequences": [
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],
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"intron_rank": 20,
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"gene_symbol": "DGKB",
"gene_hgnc_id": 2850,
"hgvs_c": "c.1647+8939T>C",
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"transcript": "NM_001350722.2",
"protein_id": "NP_001337651.1",
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"mane_select": null,
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},
{
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"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 26,
"intron_rank": 20,
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"gene_symbol": "DGKB",
"gene_hgnc_id": 2850,
"hgvs_c": "c.1647+8939T>C",
"hgvs_p": null,
"transcript": "NM_001350723.2",
"protein_id": "NP_001337652.1",
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}