Canonical Allele Identifier: CA1838420
Gene: IL36RN HGNC NCBI

Linked Data

dbSNP Id: rs767374989
ExAC: 2:113820030 C / A
gnomAD v2: 2-113820030-C-A
gnomAD v3: 2-113062453-C-A
gnomAD v4: 2-113062453-C-A
MyVariant Identifiers: chr2:g.113820030C>A (hg19) chr2:g.113062453C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113062453C>A , CM000664.2:g.113062453C>A GRCh38
NC_000002.11:g.113820030C>A , CM000664.1:g.113820030C>A GRCh37
NC_000002.10:g.113536501C>A NCBI36
NG_031864.1:g.8816C>A , LRG_730:g.8816C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.244C>A ENSP00000409262.2:p.Pro82Thr
ENST00000393200.7:c.244C>A MANE Select ENSP00000376896.2:p.Pro82Thr
ENST00000346807.7:c.244C>A ENSP00000259212.3:p.Pro82Thr
ENST00000393200.6:c.244C>A ENSP00000376896.2:p.Pro82Thr
ENST00000437409.1:c.244C>A ENSP00000409262.1:p.Pro82Thr
NM_012275.2:c.244C>A , LRG_730t2:c.244C>A NP_036407.1:p.Pro82Thr
NM_173170.1:c.244C>A , LRG_730t1:c.244C>A NP_775262.1:p.Pro82Thr
NM_012275.3:c.244C>A MANE Select NP_036407.1:p.Pro82Thr
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