Canonical Allele Identifier: CA348289982

Gene: IL36RN

Linked Data

• gnomAD v4: 2-113062147-A-T
• MyVariant Identifiers: chr2:g.113819724A>T (hg19) ; chr2:g.113062147A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113062147A>T , CM000664.2:g.113062147A>T	GRCh38
NC_000002.11:g.113819724A>T , CM000664.1:g.113819724A>T	GRCh37
NC_000002.10:g.113536195A>T	NCBI36
NG_031864.1:g.8510A>T , LRG_730:g.8510A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437409.2:c.139A>T	ENSP00000409262.2:p.Asn47Tyr
ENST00000393200.7:c.139A>T MANE Select	ENSP00000376896.2:p.Asn47Tyr
ENST00000346807.7:c.139A>T	ENSP00000259212.3:p.Asn47Tyr
ENST00000393200.6:c.139A>T	ENSP00000376896.2:p.Asn47Tyr
ENST00000437409.1:c.139A>T	ENSP00000409262.1:p.Asn47Tyr
NM_012275.2:c.139A>T , LRG_730t2:c.139A>T	NP_036407.1:p.Asn47Tyr
NM_173170.1:c.139A>T , LRG_730t1:c.139A>T	NP_775262.1:p.Asn47Tyr
NM_012275.3:c.139A>T MANE Select	NP_036407.1:p.Asn47Tyr