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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-134772210-C-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=134772210&ref=C&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "X",
"pos": 134772210,
"ref": "C",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_001331088.1",
"consequences": [
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PABIR2",
"gene_hgnc_id": 30490,
"hgvs_c": "c.733G>T",
"hgvs_p": "p.Ala245Ser",
"transcript": "NM_001387468.1",
"protein_id": "NP_001374397.1",
"transcript_support_level": null,
"aa_start": 245,
"aa_end": null,
"aa_length": 267,
"cds_start": 733,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000343004.10",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001387468.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PABIR2",
"gene_hgnc_id": 30490,
"hgvs_c": "c.733G>T",
"hgvs_p": "p.Ala245Ser",
"transcript": "ENST00000343004.10",
"protein_id": "ENSP00000339207.6",
"transcript_support_level": 1,
"aa_start": 245,
"aa_end": null,
"aa_length": 267,
"cds_start": 733,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001387468.1",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000343004.10"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PABIR2",
"gene_hgnc_id": 30490,
"hgvs_c": "c.673G>T",
"hgvs_p": "p.Ala225Ser",
"transcript": "ENST00000370790.5",
"protein_id": "ENSP00000359826.1",
"transcript_support_level": 1,
"aa_start": 225,
"aa_end": null,
"aa_length": 247,
"cds_start": 673,
"cds_end": null,
"cds_length": 744,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000370790.5"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PABIR2",
"gene_hgnc_id": 30490,
"hgvs_c": "c.745G>T",
"hgvs_p": "p.Ala249Ser",
"transcript": "NM_001331088.1",
"protein_id": "NP_001318017.1",
"transcript_support_level": null,
"aa_start": 249,
"aa_end": null,
"aa_length": 271,
"cds_start": 745,
"cds_end": null,
"cds_length": 816,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001331088.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PABIR2",
"gene_hgnc_id": 30490,
"hgvs_c": "c.742G>T",
"hgvs_p": "p.Ala248Ser",
"transcript": "NM_001331089.1",
"protein_id": "NP_001318018.1",
"transcript_support_level": null,
"aa_start": 248,
"aa_end": null,
"aa_length": 270,
"cds_start": 742,
"cds_end": null,
"cds_length": 813,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001331089.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PABIR2",
"gene_hgnc_id": 30490,
"hgvs_c": "c.742G>T",
"hgvs_p": "p.Ala248Ser",
"transcript": "ENST00000896544.1",
"protein_id": "ENSP00000566603.1",
"transcript_support_level": null,
"aa_start": 248,
"aa_end": null,
"aa_length": 270,
"cds_start": 742,
"cds_end": null,
"cds_length": 813,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000896544.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PABIR2",
"gene_hgnc_id": 30490,
"hgvs_c": "c.733G>T",
"hgvs_p": "p.Ala245Ser",
"transcript": "ENST00000611027.2",
"protein_id": "ENSP00000479150.2",
"transcript_support_level": 5,
"aa_start": 245,
"aa_end": null,
"aa_length": 267,
"cds_start": 733,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000611027.2"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PABIR2",
"gene_hgnc_id": 30490,
"hgvs_c": "c.730G>T",
"hgvs_p": "p.Ala244Ser",
"transcript": "NM_001170756.1",
"protein_id": "NP_001164227.1",
"transcript_support_level": null,
"aa_start": 244,
"aa_end": null,
"aa_length": 266,
"cds_start": 730,
"cds_end": null,
"cds_length": 801,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001170756.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PABIR2",
"gene_hgnc_id": 30490,
"hgvs_c": "c.730G>T",
"hgvs_p": "p.Ala244Ser",
"transcript": "ENST00000493333.5",
"protein_id": "ENSP00000487221.1",
"transcript_support_level": 5,
"aa_start": 244,
"aa_end": null,
"aa_length": 266,
"cds_start": 730,
"cds_end": null,
"cds_length": 801,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000493333.5"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PABIR2",
"gene_hgnc_id": 30490,
"hgvs_c": "c.730G>T",
"hgvs_p": "p.Ala244Ser",
"transcript": "ENST00000896543.1",
"protein_id": "ENSP00000566602.1",
"transcript_support_level": null,
"aa_start": 244,
"aa_end": null,
"aa_length": 266,
"cds_start": 730,
"cds_end": null,
"cds_length": 801,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000896543.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PABIR2",
"gene_hgnc_id": 30490,
"hgvs_c": "c.685G>T",
"hgvs_p": "p.Ala229Ser",
"transcript": "ENST00000896545.1",
"protein_id": "ENSP00000566604.1",
"transcript_support_level": null,
"aa_start": 229,
"aa_end": null,
"aa_length": 251,
"cds_start": 685,
"cds_end": null,
"cds_length": 756,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000896545.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PABIR2",
"gene_hgnc_id": 30490,
"hgvs_c": "c.676G>T",
"hgvs_p": "p.Ala226Ser",
"transcript": "NM_145284.5",
"protein_id": "NP_660327.2",
"transcript_support_level": null,
"aa_start": 226,
"aa_end": null,
"aa_length": 248,
"cds_start": 676,
"cds_end": null,
"cds_length": 747,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_145284.5"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PABIR2",
"gene_hgnc_id": 30490,
"hgvs_c": "c.676G>T",
"hgvs_p": "p.Ala226Ser",
"transcript": "ENST00000486347.5",
"protein_id": "ENSP00000419592.1",
"transcript_support_level": 2,
"aa_start": 226,
"aa_end": null,
"aa_length": 248,
"cds_start": 676,
"cds_end": null,
"cds_length": 747,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000486347.5"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PABIR2",
"gene_hgnc_id": 30490,
"hgvs_c": "c.673G>T",
"hgvs_p": "p.Ala225Ser",
"transcript": "NM_001166599.3",
"protein_id": "NP_001160071.1",
"transcript_support_level": null,
"aa_start": 225,
"aa_end": null,
"aa_length": 247,
"cds_start": 673,
"cds_end": null,
"cds_length": 744,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001166599.3"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PABIR2",
"gene_hgnc_id": 30490,
"hgvs_c": "c.745G>T",
"hgvs_p": "p.Ala249Ser",
"transcript": "XM_011531282.3",
"protein_id": "XP_011529584.1",
"transcript_support_level": null,
"aa_start": 249,
"aa_end": null,
"aa_length": 293,
"cds_start": 745,
"cds_end": null,
"cds_length": 882,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011531282.3"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PABIR2",
"gene_hgnc_id": 30490,
"hgvs_c": "c.742G>T",
"hgvs_p": "p.Ala248Ser",
"transcript": "XM_011531283.3",
"protein_id": "XP_011529585.1",
"transcript_support_level": null,
"aa_start": 248,
"aa_end": null,
"aa_length": 292,
"cds_start": 742,
"cds_end": null,
"cds_length": 879,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011531283.3"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PABIR2",
"gene_hgnc_id": 30490,
"hgvs_c": "c.733G>T",
"hgvs_p": "p.Ala245Ser",
"transcript": "XM_011531284.3",
"protein_id": "XP_011529586.1",
"transcript_support_level": null,
"aa_start": 245,
"aa_end": null,
"aa_length": 289,
"cds_start": 733,
"cds_end": null,
"cds_length": 870,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011531284.3"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PABIR2",
"gene_hgnc_id": 30490,
"hgvs_c": "c.730G>T",
"hgvs_p": "p.Ala244Ser",
"transcript": "XM_011531285.3",
"protein_id": "XP_011529587.1",
"transcript_support_level": null,
"aa_start": 244,
"aa_end": null,
"aa_length": 288,
"cds_start": 730,
"cds_end": null,
"cds_length": 867,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011531285.3"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PABIR2",
"gene_hgnc_id": 30490,
"hgvs_c": "c.688G>T",
"hgvs_p": "p.Ala230Ser",
"transcript": "XM_011531286.3",
"protein_id": "XP_011529588.1",
"transcript_support_level": null,
"aa_start": 230,
"aa_end": null,
"aa_length": 274,
"cds_start": 688,
"cds_end": null,
"cds_length": 825,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011531286.3"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PABIR2",
"gene_hgnc_id": 30490,
"hgvs_c": "c.685G>T",
"hgvs_p": "p.Ala229Ser",
"transcript": "XM_047441873.1",
"protein_id": "XP_047297829.1",
"transcript_support_level": null,
"aa_start": 229,
"aa_end": null,
"aa_length": 273,
"cds_start": 685,
"cds_end": null,
"cds_length": 822,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047441873.1"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PABIR2",
"gene_hgnc_id": 30490,
"hgvs_c": "c.676G>T",
"hgvs_p": "p.Ala226Ser",
"transcript": "XM_011531288.3",
"protein_id": "XP_011529590.1",
"transcript_support_level": null,
"aa_start": 226,
"aa_end": null,
"aa_length": 270,
"cds_start": 676,
"cds_end": null,
"cds_length": 813,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011531288.3"
},
{
"aa_ref": "A",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PABIR2",
"gene_hgnc_id": 30490,
"hgvs_c": "c.673G>T",
"hgvs_p": "p.Ala225Ser",
"transcript": "XM_011531290.3",
"protein_id": "XP_011529592.1",
"transcript_support_level": null,
"aa_start": 225,
"aa_end": null,
"aa_length": 269,
"cds_start": 673,
"cds_end": null,
"cds_length": 810,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
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}