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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: 4-7984886-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=4&pos=7984886&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "4",
"pos": 7984886,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_001130083.2",
"consequences": [
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABLIM2",
"gene_hgnc_id": 19195,
"hgvs_c": "c.1688A>G",
"hgvs_p": "p.Asn563Ser",
"transcript": "NM_001130083.2",
"protein_id": "NP_001123555.1",
"transcript_support_level": null,
"aa_start": 563,
"aa_end": null,
"aa_length": 645,
"cds_start": 1688,
"cds_end": null,
"cds_length": 1938,
"cdna_start": 1812,
"cdna_end": null,
"cdna_length": 3725,
"mane_select": "ENST00000447017.7",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001130083.2"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABLIM2",
"gene_hgnc_id": 19195,
"hgvs_c": "c.1688A>G",
"hgvs_p": "p.Asn563Ser",
"transcript": "ENST00000447017.7",
"protein_id": "ENSP00000393511.2",
"transcript_support_level": 1,
"aa_start": 563,
"aa_end": null,
"aa_length": 645,
"cds_start": 1688,
"cds_end": null,
"cds_length": 1938,
"cdna_start": 1812,
"cdna_end": null,
"cdna_length": 3725,
"mane_select": "NM_001130083.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000447017.7"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABLIM2",
"gene_hgnc_id": 19195,
"hgvs_c": "c.1586A>G",
"hgvs_p": "p.Asn529Ser",
"transcript": "ENST00000341937.9",
"protein_id": "ENSP00000342813.5",
"transcript_support_level": 1,
"aa_start": 529,
"aa_end": null,
"aa_length": 611,
"cds_start": 1586,
"cds_end": null,
"cds_length": 1836,
"cdna_start": 1651,
"cdna_end": null,
"cdna_length": 2589,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000341937.9"
},
{
"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": 18,
"intron_rank": 15,
"intron_rank_end": null,
"gene_symbol": "ABLIM2",
"gene_hgnc_id": 19195,
"hgvs_c": "c.1517-1332A>G",
"hgvs_p": null,
"transcript": "ENST00000361581.9",
"protein_id": "ENSP00000355003.5",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 572,
"cds_start": null,
"cds_end": null,
"cds_length": 1719,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2472,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000361581.9"
},
{
"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": 16,
"intron_rank": 13,
"intron_rank_end": null,
"gene_symbol": "ABLIM2",
"gene_hgnc_id": 19195,
"hgvs_c": "c.1364-1332A>G",
"hgvs_p": null,
"transcript": "ENST00000407564.7",
"protein_id": "ENSP00000384658.3",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 521,
"cds_start": null,
"cds_end": null,
"cds_length": 1566,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2291,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000407564.7"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABLIM2",
"gene_hgnc_id": 19195,
"hgvs_c": "c.1808A>G",
"hgvs_p": "p.Asn603Ser",
"transcript": "ENST00000710854.1",
"protein_id": "ENSP00000518527.1",
"transcript_support_level": null,
"aa_start": 603,
"aa_end": null,
"aa_length": 685,
"cds_start": 1808,
"cds_end": null,
"cds_length": 2058,
"cdna_start": 1932,
"cdna_end": null,
"cdna_length": 3845,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000710854.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABLIM2",
"gene_hgnc_id": 19195,
"hgvs_c": "c.1703A>G",
"hgvs_p": "p.Asn568Ser",
"transcript": "ENST00000545242.6",
"protein_id": "ENSP00000441255.3",
"transcript_support_level": 5,
"aa_start": 568,
"aa_end": null,
"aa_length": 650,
"cds_start": 1703,
"cds_end": null,
"cds_length": 1953,
"cdna_start": 1792,
"cdna_end": null,
"cdna_length": 2986,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000545242.6"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABLIM2",
"gene_hgnc_id": 19195,
"hgvs_c": "c.1634A>G",
"hgvs_p": "p.Asn545Ser",
"transcript": "ENST00000676532.1",
"protein_id": "ENSP00000504601.1",
"transcript_support_level": null,
"aa_start": 545,
"aa_end": null,
"aa_length": 627,
"cds_start": 1634,
"cds_end": null,
"cds_length": 1884,
"cdna_start": 1733,
"cdna_end": null,
"cdna_length": 3661,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000676532.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABLIM2",
"gene_hgnc_id": 19195,
"hgvs_c": "c.1586A>G",
"hgvs_p": "p.Asn529Ser",
"transcript": "NM_001130084.2",
"protein_id": "NP_001123556.1",
"transcript_support_level": null,
"aa_start": 529,
"aa_end": null,
"aa_length": 611,
"cds_start": 1586,
"cds_end": null,
"cds_length": 1836,
"cdna_start": 1710,
"cdna_end": null,
"cdna_length": 3623,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001130084.2"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABLIM2",
"gene_hgnc_id": 19195,
"hgvs_c": "c.1430A>G",
"hgvs_p": "p.Asn477Ser",
"transcript": "NM_001130086.2",
"protein_id": "NP_001123558.1",
"transcript_support_level": null,
"aa_start": 477,
"aa_end": null,
"aa_length": 559,
"cds_start": 1430,
"cds_end": null,
"cds_length": 1680,
"cdna_start": 1554,
"cdna_end": null,
"cdna_length": 3467,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001130086.2"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABLIM2",
"gene_hgnc_id": 19195,
"hgvs_c": "c.1430A>G",
"hgvs_p": "p.Asn477Ser",
"transcript": "ENST00000505872.5",
"protein_id": "ENSP00000421283.1",
"transcript_support_level": 5,
"aa_start": 477,
"aa_end": null,
"aa_length": 559,
"cds_start": 1430,
"cds_end": null,
"cds_length": 1680,
"cdna_start": 1430,
"cdna_end": null,
"cdna_length": 1680,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000505872.5"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABLIM2",
"gene_hgnc_id": 19195,
"hgvs_c": "c.791A>G",
"hgvs_p": "p.Asn264Ser",
"transcript": "NM_001286688.2",
"protein_id": "NP_001273617.1",
"transcript_support_level": null,
"aa_start": 264,
"aa_end": null,
"aa_length": 346,
"cds_start": 791,
"cds_end": null,
"cds_length": 1041,
"cdna_start": 1065,
"cdna_end": null,
"cdna_length": 2978,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001286688.2"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABLIM2",
"gene_hgnc_id": 19195,
"hgvs_c": "c.791A>G",
"hgvs_p": "p.Asn264Ser",
"transcript": "ENST00000514025.5",
"protein_id": "ENSP00000423661.1",
"transcript_support_level": 2,
"aa_start": 264,
"aa_end": null,
"aa_length": 346,
"cds_start": 791,
"cds_end": null,
"cds_length": 1041,
"cdna_start": 1063,
"cdna_end": null,
"cdna_length": 2974,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000514025.5"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABLIM2",
"gene_hgnc_id": 19195,
"hgvs_c": "c.1979A>G",
"hgvs_p": "p.Asn660Ser",
"transcript": "XM_047416297.1",
"protein_id": "XP_047272253.1",
"transcript_support_level": null,
"aa_start": 660,
"aa_end": null,
"aa_length": 742,
"cds_start": 1979,
"cds_end": null,
"cds_length": 2229,
"cdna_start": 2068,
"cdna_end": null,
"cdna_length": 3981,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047416297.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABLIM2",
"gene_hgnc_id": 19195,
"hgvs_c": "c.1976A>G",
"hgvs_p": "p.Asn659Ser",
"transcript": "XM_047416298.1",
"protein_id": "XP_047272254.1",
"transcript_support_level": null,
"aa_start": 659,
"aa_end": null,
"aa_length": 741,
"cds_start": 1976,
"cds_end": null,
"cds_length": 2226,
"cdna_start": 2065,
"cdna_end": null,
"cdna_length": 3978,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047416298.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABLIM2",
"gene_hgnc_id": 19195,
"hgvs_c": "c.1964A>G",
"hgvs_p": "p.Asn655Ser",
"transcript": "XM_047416299.1",
"protein_id": "XP_047272255.1",
"transcript_support_level": null,
"aa_start": 655,
"aa_end": null,
"aa_length": 737,
"cds_start": 1964,
"cds_end": null,
"cds_length": 2214,
"cdna_start": 2088,
"cdna_end": null,
"cdna_length": 4001,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047416299.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABLIM2",
"gene_hgnc_id": 19195,
"hgvs_c": "c.1946A>G",
"hgvs_p": "p.Asn649Ser",
"transcript": "XM_047416300.1",
"protein_id": "XP_047272256.1",
"transcript_support_level": null,
"aa_start": 649,
"aa_end": null,
"aa_length": 731,
"cds_start": 1946,
"cds_end": null,
"cds_length": 2196,
"cdna_start": 2035,
"cdna_end": null,
"cdna_length": 3948,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047416300.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABLIM2",
"gene_hgnc_id": 19195,
"hgvs_c": "c.1931A>G",
"hgvs_p": "p.Asn644Ser",
"transcript": "XM_047416301.1",
"protein_id": "XP_047272257.1",
"transcript_support_level": null,
"aa_start": 644,
"aa_end": null,
"aa_length": 726,
"cds_start": 1931,
"cds_end": null,
"cds_length": 2181,
"cdna_start": 2055,
"cdna_end": null,
"cdna_length": 3968,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047416301.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABLIM2",
"gene_hgnc_id": 19195,
"hgvs_c": "c.1880A>G",
"hgvs_p": "p.Asn627Ser",
"transcript": "XM_047416302.1",
"protein_id": "XP_047272258.1",
"transcript_support_level": null,
"aa_start": 627,
"aa_end": null,
"aa_length": 709,
"cds_start": 1880,
"cds_end": null,
"cds_length": 2130,
"cdna_start": 1969,
"cdna_end": null,
"cdna_length": 3882,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047416302.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABLIM2",
"gene_hgnc_id": 19195,
"hgvs_c": "c.1859A>G",
"hgvs_p": "p.Asn620Ser",
"transcript": "XM_047416303.1",
"protein_id": "XP_047272259.1",
"transcript_support_level": null,
"aa_start": 620,
"aa_end": null,
"aa_length": 702,
"cds_start": 1859,
"cds_end": null,
"cds_length": 2109,
"cdna_start": 1948,
"cdna_end": null,
"cdna_length": 3861,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047416303.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABLIM2",
"gene_hgnc_id": 19195,
"hgvs_c": "c.1856A>G",
"hgvs_p": "p.Asn619Ser",
"transcript": "XM_005248014.6",
"protein_id": "XP_005248071.1",
"transcript_support_level": null,
"aa_start": 619,
"aa_end": null,
"aa_length": 701,
"cds_start": 1856,
"cds_end": null,
"cds_length": 2106,
"cdna_start": 1945,
"cdna_end": null,
"cdna_length": 3858,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_005248014.6"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABLIM2",
"gene_hgnc_id": 19195,
"hgvs_c": "c.1856A>G",
"hgvs_p": "p.Asn619Ser",
"transcript": "XM_047416305.1",
"protein_id": "XP_047272261.1",
"transcript_support_level": null,
"aa_start": 619,
"aa_end": null,
"aa_length": 701,
"cds_start": 1856,
"cds_end": null,
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}
],
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}