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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: 2-170335435-A-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=170335435&ref=A&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 170335435,
"ref": "A",
"alt": "T",
"effect": "missense_variant",
"transcript": "ENST00000408978.9",
"consequences": [
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "c.800A>T",
"hgvs_p": "p.Asn267Ile",
"transcript": "NM_138995.5",
"protein_id": "NP_620482.3",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 1341,
"cds_start": 800,
"cds_end": null,
"cds_length": 4026,
"cdna_start": 941,
"cdna_end": null,
"cdna_length": 6213,
"mane_select": "ENST00000408978.9",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "c.800A>T",
"hgvs_p": "p.Asn267Ile",
"transcript": "ENST00000408978.9",
"protein_id": "ENSP00000386213.4",
"transcript_support_level": 1,
"aa_start": 267,
"aa_end": null,
"aa_length": 1341,
"cds_start": 800,
"cds_end": null,
"cds_length": 4026,
"cdna_start": 941,
"cdna_end": null,
"cdna_length": 6213,
"mane_select": "NM_138995.5",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "c.800A>T",
"hgvs_p": "p.Asn267Ile",
"transcript": "ENST00000409044.7",
"protein_id": "ENSP00000386497.3",
"transcript_support_level": 1,
"aa_start": 267,
"aa_end": null,
"aa_length": 1314,
"cds_start": 800,
"cds_end": null,
"cds_length": 3945,
"cdna_start": 943,
"cdna_end": null,
"cdna_length": 5448,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "c.797A>T",
"hgvs_p": "p.Asn266Ile",
"transcript": "ENST00000442690.1",
"protein_id": "ENSP00000401160.1",
"transcript_support_level": 1,
"aa_start": 266,
"aa_end": null,
"aa_length": 359,
"cds_start": 797,
"cds_end": null,
"cds_length": 1080,
"cdna_start": 798,
"cdna_end": null,
"cdna_length": 1720,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "n.943A>T",
"hgvs_p": null,
"transcript": "ENST00000409940.6",
"protein_id": null,
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4156,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "c.800A>T",
"hgvs_p": "p.Asn267Ile",
"transcript": "NM_001083615.4",
"protein_id": "NP_001077084.2",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 1314,
"cds_start": 800,
"cds_end": null,
"cds_length": 3945,
"cdna_start": 941,
"cdna_end": null,
"cdna_length": 6132,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "c.827A>T",
"hgvs_p": "p.Asn276Ile",
"transcript": "ENST00000484338.6",
"protein_id": "ENSP00000446237.1",
"transcript_support_level": 5,
"aa_start": 276,
"aa_end": null,
"aa_length": 1104,
"cds_start": 827,
"cds_end": null,
"cds_length": 3316,
"cdna_start": 831,
"cdna_end": null,
"cdna_length": 3320,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "c.827A>T",
"hgvs_p": "p.Asn276Ile",
"transcript": "XM_011510654.4",
"protein_id": "XP_011508956.1",
"transcript_support_level": null,
"aa_start": 276,
"aa_end": null,
"aa_length": 1386,
"cds_start": 827,
"cds_end": null,
"cds_length": 4161,
"cdna_start": 850,
"cdna_end": null,
"cdna_length": 6230,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "c.827A>T",
"hgvs_p": "p.Asn276Ile",
"transcript": "XM_006712299.5",
"protein_id": "XP_006712362.1",
"transcript_support_level": null,
"aa_start": 276,
"aa_end": null,
"aa_length": 1350,
"cds_start": 827,
"cds_end": null,
"cds_length": 4053,
"cdna_start": 850,
"cdna_end": null,
"cdna_length": 6122,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "N",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "c.827A>T",
"hgvs_p": "p.Asn276Ile",
"transcript": "XM_011510655.4",
"protein_id": "XP_011508957.1",
"transcript_support_level": null,
"aa_start": 276,
"aa_end": null,
"aa_length": 1323,
"cds_start": 827,
"cds_end": null,
"cds_length": 3972,
"cdna_start": 850,
"cdna_end": null,
"cdna_length": 6041,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "n.800A>T",
"hgvs_p": null,
"transcript": "ENST00000317935.10",
"protein_id": "ENSP00000314650.6",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5479,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "n.943A>T",
"hgvs_p": null,
"transcript": "ENST00000438642.6",
"protein_id": null,
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4010,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "n.654A>T",
"hgvs_p": null,
"transcript": "ENST00000602629.1",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5304,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "n.941A>T",
"hgvs_p": null,
"transcript": "NR_045682.2",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
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"cdna_start": null,
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"cdna_length": 6335,
"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "n.941A>T",
"hgvs_p": null,
"transcript": "NR_045683.2",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
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"cdna_start": null,
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"cdna_length": 6244,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYO3B",
"gene_hgnc_id": 15576,
"hgvs_c": "n.941A>T",
"hgvs_p": null,
"transcript": "NR_045684.2",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "MYO3B-AS1",
"gene_hgnc_id": 40713,
"hgvs_c": "n.491-556T>A",
"hgvs_p": null,
"transcript": "ENST00000593578.6",
"protein_id": null,
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
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"cds_length": null,
"cdna_start": null,
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"cdna_length": 743,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "MYO3B-AS1",
"gene_hgnc_id": 40713,
"hgvs_c": "n.657-556T>A",
"hgvs_p": null,
"transcript": "ENST00000593861.5",
"protein_id": null,
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
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"cdna_start": null,
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"cdna_length": 771,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "MYO3B-AS1",
"gene_hgnc_id": 40713,
"hgvs_c": "n.556-556T>A",
"hgvs_p": null,
"transcript": "ENST00000594762.5",
"protein_id": null,
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"aa_start": null,
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"biotype": null,
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},
{
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"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 6,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "MYO3B-AS1",
"gene_hgnc_id": 40713,
"hgvs_c": "n.435-556T>A",
"hgvs_p": null,
"transcript": "ENST00000595528.5",
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"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
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"cds_start": -4,
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"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "MYO3B-AS1",
"gene_hgnc_id": 40713,
"hgvs_c": "n.375-556T>A",
"hgvs_p": null,
"transcript": "ENST00000597915.5",
"protein_id": null,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "MYO3B-AS1",
"gene_hgnc_id": 40713,
"hgvs_c": "n.394-556T>A",
"hgvs_p": null,
"transcript": "ENST00000599635.5",
"protein_id": null,
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
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"cdna_length": 766,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "MYO3B-AS1",
"gene_hgnc_id": 40713,
"hgvs_c": "n.645-556T>A",
"hgvs_p": null,
"transcript": "ENST00000600365.5",
"protein_id": null,
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
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"cds_length": null,
"cdna_start": null,
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"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}