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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: 19-35870936-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=35870936&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "19",
"pos": 35870936,
"ref": "C",
"alt": "G",
"effect": "missense_variant",
"transcript": "NM_001024807.3",
"consequences": [
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "APLP1",
"gene_hgnc_id": 597,
"hgvs_c": "c.332C>G",
"hgvs_p": "p.Thr111Arg",
"transcript": "NM_001024807.3",
"protein_id": "NP_001019978.1",
"transcript_support_level": null,
"aa_start": 111,
"aa_end": null,
"aa_length": 651,
"cds_start": 332,
"cds_end": null,
"cds_length": 1956,
"cdna_start": 395,
"cdna_end": null,
"cdna_length": 2370,
"mane_select": "ENST00000221891.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001024807.3"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "APLP1",
"gene_hgnc_id": 597,
"hgvs_c": "c.332C>G",
"hgvs_p": "p.Thr111Arg",
"transcript": "ENST00000221891.9",
"protein_id": "ENSP00000221891.4",
"transcript_support_level": 1,
"aa_start": 111,
"aa_end": null,
"aa_length": 651,
"cds_start": 332,
"cds_end": null,
"cds_length": 1956,
"cdna_start": 395,
"cdna_end": null,
"cdna_length": 2370,
"mane_select": "NM_001024807.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000221891.9"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "APLP1",
"gene_hgnc_id": 597,
"hgvs_c": "c.332C>G",
"hgvs_p": "p.Thr111Arg",
"transcript": "ENST00000960045.1",
"protein_id": "ENSP00000630104.1",
"transcript_support_level": null,
"aa_start": 111,
"aa_end": null,
"aa_length": 673,
"cds_start": 332,
"cds_end": null,
"cds_length": 2022,
"cdna_start": 456,
"cdna_end": null,
"cdna_length": 2501,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000960045.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "APLP1",
"gene_hgnc_id": 597,
"hgvs_c": "c.332C>G",
"hgvs_p": "p.Thr111Arg",
"transcript": "ENST00000898023.1",
"protein_id": "ENSP00000568082.1",
"transcript_support_level": null,
"aa_start": 111,
"aa_end": null,
"aa_length": 655,
"cds_start": 332,
"cds_end": null,
"cds_length": 1968,
"cdna_start": 445,
"cdna_end": null,
"cdna_length": 2432,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898023.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "APLP1",
"gene_hgnc_id": 597,
"hgvs_c": "c.332C>G",
"hgvs_p": "p.Thr111Arg",
"transcript": "ENST00000898026.1",
"protein_id": "ENSP00000568085.1",
"transcript_support_level": null,
"aa_start": 111,
"aa_end": null,
"aa_length": 654,
"cds_start": 332,
"cds_end": null,
"cds_length": 1965,
"cdna_start": 431,
"cdna_end": null,
"cdna_length": 2420,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898026.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "APLP1",
"gene_hgnc_id": 597,
"hgvs_c": "c.332C>G",
"hgvs_p": "p.Thr111Arg",
"transcript": "NM_005166.5",
"protein_id": "NP_005157.1",
"transcript_support_level": null,
"aa_start": 111,
"aa_end": null,
"aa_length": 650,
"cds_start": 332,
"cds_end": null,
"cds_length": 1953,
"cdna_start": 395,
"cdna_end": null,
"cdna_length": 2367,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_005166.5"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "APLP1",
"gene_hgnc_id": 597,
"hgvs_c": "c.332C>G",
"hgvs_p": "p.Thr111Arg",
"transcript": "ENST00000652533.2",
"protein_id": "ENSP00000498366.1",
"transcript_support_level": null,
"aa_start": 111,
"aa_end": null,
"aa_length": 650,
"cds_start": 332,
"cds_end": null,
"cds_length": 1953,
"cdna_start": 373,
"cdna_end": null,
"cdna_length": 2356,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000652533.2"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "APLP1",
"gene_hgnc_id": 597,
"hgvs_c": "c.332C>G",
"hgvs_p": "p.Thr111Arg",
"transcript": "ENST00000898022.1",
"protein_id": "ENSP00000568081.1",
"transcript_support_level": null,
"aa_start": 111,
"aa_end": null,
"aa_length": 648,
"cds_start": 332,
"cds_end": null,
"cds_length": 1947,
"cdna_start": 439,
"cdna_end": null,
"cdna_length": 2413,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898022.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "APLP1",
"gene_hgnc_id": 597,
"hgvs_c": "c.332C>G",
"hgvs_p": "p.Thr111Arg",
"transcript": "ENST00000898029.1",
"protein_id": "ENSP00000568088.1",
"transcript_support_level": null,
"aa_start": 111,
"aa_end": null,
"aa_length": 648,
"cds_start": 332,
"cds_end": null,
"cds_length": 1947,
"cdna_start": 393,
"cdna_end": null,
"cdna_length": 2359,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898029.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "APLP1",
"gene_hgnc_id": 597,
"hgvs_c": "c.332C>G",
"hgvs_p": "p.Thr111Arg",
"transcript": "ENST00000898020.1",
"protein_id": "ENSP00000568079.1",
"transcript_support_level": null,
"aa_start": 111,
"aa_end": null,
"aa_length": 647,
"cds_start": 332,
"cds_end": null,
"cds_length": 1944,
"cdna_start": 450,
"cdna_end": null,
"cdna_length": 2424,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898020.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "APLP1",
"gene_hgnc_id": 597,
"hgvs_c": "c.332C>G",
"hgvs_p": "p.Thr111Arg",
"transcript": "ENST00000898034.1",
"protein_id": "ENSP00000568093.1",
"transcript_support_level": null,
"aa_start": 111,
"aa_end": null,
"aa_length": 647,
"cds_start": 332,
"cds_end": null,
"cds_length": 1944,
"cdna_start": 393,
"cdna_end": null,
"cdna_length": 2354,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898034.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "APLP1",
"gene_hgnc_id": 597,
"hgvs_c": "c.332C>G",
"hgvs_p": "p.Thr111Arg",
"transcript": "ENST00000912740.1",
"protein_id": "ENSP00000582799.1",
"transcript_support_level": null,
"aa_start": 111,
"aa_end": null,
"aa_length": 646,
"cds_start": 332,
"cds_end": null,
"cds_length": 1941,
"cdna_start": 431,
"cdna_end": null,
"cdna_length": 2394,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000912740.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "APLP1",
"gene_hgnc_id": 597,
"hgvs_c": "c.314C>G",
"hgvs_p": "p.Thr105Arg",
"transcript": "ENST00000586861.5",
"protein_id": "ENSP00000465694.1",
"transcript_support_level": 2,
"aa_start": 105,
"aa_end": null,
"aa_length": 644,
"cds_start": 314,
"cds_end": null,
"cds_length": 1935,
"cdna_start": 379,
"cdna_end": null,
"cdna_length": 2052,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000586861.5"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "APLP1",
"gene_hgnc_id": 597,
"hgvs_c": "c.332C>G",
"hgvs_p": "p.Thr111Arg",
"transcript": "ENST00000898030.1",
"protein_id": "ENSP00000568089.1",
"transcript_support_level": null,
"aa_start": 111,
"aa_end": null,
"aa_length": 639,
"cds_start": 332,
"cds_end": null,
"cds_length": 1920,
"cdna_start": 393,
"cdna_end": null,
"cdna_length": 2332,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898030.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "APLP1",
"gene_hgnc_id": 597,
"hgvs_c": "c.332C>G",
"hgvs_p": "p.Thr111Arg",
"transcript": "ENST00000898032.1",
"protein_id": "ENSP00000568091.1",
"transcript_support_level": null,
"aa_start": 111,
"aa_end": null,
"aa_length": 638,
"cds_start": 332,
"cds_end": null,
"cds_length": 1917,
"cdna_start": 393,
"cdna_end": null,
"cdna_length": 2329,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898032.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "APLP1",
"gene_hgnc_id": 597,
"hgvs_c": "c.332C>G",
"hgvs_p": "p.Thr111Arg",
"transcript": "ENST00000960049.1",
"protein_id": "ENSP00000630108.1",
"transcript_support_level": null,
"aa_start": 111,
"aa_end": null,
"aa_length": 637,
"cds_start": 332,
"cds_end": null,
"cds_length": 1914,
"cdna_start": 379,
"cdna_end": null,
"cdna_length": 2311,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000960049.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "APLP1",
"gene_hgnc_id": 597,
"hgvs_c": "c.332C>G",
"hgvs_p": "p.Thr111Arg",
"transcript": "ENST00000898033.1",
"protein_id": "ENSP00000568092.1",
"transcript_support_level": null,
"aa_start": 111,
"aa_end": null,
"aa_length": 632,
"cds_start": 332,
"cds_end": null,
"cds_length": 1899,
"cdna_start": 393,
"cdna_end": null,
"cdna_length": 2311,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898033.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "APLP1",
"gene_hgnc_id": 597,
"hgvs_c": "c.332C>G",
"hgvs_p": "p.Thr111Arg",
"transcript": "ENST00000898028.1",
"protein_id": "ENSP00000568087.1",
"transcript_support_level": null,
"aa_start": 111,
"aa_end": null,
"aa_length": 630,
"cds_start": 332,
"cds_end": null,
"cds_length": 1893,
"cdna_start": 393,
"cdna_end": null,
"cdna_length": 2306,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898028.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "APLP1",
"gene_hgnc_id": 597,
"hgvs_c": "c.332C>G",
"hgvs_p": "p.Thr111Arg",
"transcript": "ENST00000898024.1",
"protein_id": "ENSP00000568083.1",
"transcript_support_level": null,
"aa_start": 111,
"aa_end": null,
"aa_length": 629,
"cds_start": 332,
"cds_end": null,
"cds_length": 1890,
"cdna_start": 440,
"cdna_end": null,
"cdna_length": 2352,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898024.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "APLP1",
"gene_hgnc_id": 597,
"hgvs_c": "c.332C>G",
"hgvs_p": "p.Thr111Arg",
"transcript": "ENST00000898031.1",
"protein_id": "ENSP00000568090.1",
"transcript_support_level": null,
"aa_start": 111,
"aa_end": null,
"aa_length": 614,
"cds_start": 332,
"cds_end": null,
"cds_length": 1845,
"cdna_start": 393,
"cdna_end": null,
"cdna_length": 2257,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000898031.1"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "APLP1",
"gene_hgnc_id": 597,
"hgvs_c": "c.215C>G",
"hgvs_p": "p.Thr72Arg",
"transcript": "ENST00000537454.6",
"protein_id": "ENSP00000441501.1",
"transcript_support_level": 2,
"aa_start": 72,
"aa_end": null,
"aa_length": 611,
"cds_start": 215,
"cds_end": null,
"cds_length": 1836,
"cdna_start": 560,
"cdna_end": null,
"cdna_length": 2266,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000537454.6"
},
{
"aa_ref": "T",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "APLP1",
"gene_hgnc_id": 597,
"hgvs_c": "c.332C>G",
"hgvs_p": "p.Thr111Arg",
"transcript": "ENST00000960046.1",
"protein_id": "ENSP00000630105.1",
"transcript_support_level": null,
"aa_start": 111,
"aa_end": null,
"aa_length": 611,
"cds_start": 332,
"cds_end": null,
"cds_length": 1836,
"cdna_start": 434,
"cdna_end": null,
"cdna_length": 2283,
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}