Canonical Allele Identifier: CA348289983

Gene: IL36RN

Linked Data

• dbSNP Id: rs28938777
• gnomAD v3: 2-113062148-A-C
• gnomAD v4: 2-113062148-A-C
• MyVariant Identifiers: chr2:g.113819725A>C (hg19) ; chr2:g.113062148A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113062148A>C , CM000664.2:g.113062148A>C	GRCh38
NC_000002.11:g.113819725A>C , CM000664.1:g.113819725A>C	GRCh37
NC_000002.10:g.113536196A>C	NCBI36
NG_031864.1:g.8511A>C , LRG_730:g.8511A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437409.2:c.140A>C	ENSP00000409262.2:p.Asn47Thr
ENST00000393200.7:c.140A>C MANE Select	ENSP00000376896.2:p.Asn47Thr
ENST00000346807.7:c.140A>C	ENSP00000259212.3:p.Asn47Thr
ENST00000393200.6:c.140A>C	ENSP00000376896.2:p.Asn47Thr
ENST00000437409.1:c.140A>C	ENSP00000409262.1:p.Asn47Thr
NM_012275.2:c.140A>C , LRG_730t2:c.140A>C	NP_036407.1:p.Asn47Thr
NM_173170.1:c.140A>C , LRG_730t1:c.140A>C	NP_775262.1:p.Asn47Thr
NM_012275.3:c.140A>C MANE Select	NP_036407.1:p.Asn47Thr