Canonical Allele Identifier: CA428300128

Gene: IL36RN

Linked Data

• MyVariant Identifiers: chr2:g.113819816T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113062239T>C , CM000664.2:g.113062239T>C	GRCh38
NC_000002.11:g.113819816T>C , CM000664.1:g.113819816T>C	GRCh37
NC_000002.10:g.113536287T>C	NCBI36
NG_031864.1:g.8602T>C , LRG_730:g.8602T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437409.2:c.231T>C	ENSP00000409262.2:p.Thr77=
ENST00000393200.7:c.231T>C MANE Select	ENSP00000376896.2:p.Thr77=
ENST00000346807.7:c.231T>C	ENSP00000259212.3:p.Thr77=
ENST00000393200.6:c.231T>C	ENSP00000376896.2:p.Thr77=
ENST00000437409.1:c.231T>C	ENSP00000409262.1:p.Thr77=
NM_012275.2:c.231T>C , LRG_730t2:c.231T>C	NP_036407.1:p.Thr77=
NM_173170.1:c.231T>C , LRG_730t1:c.231T>C	NP_775262.1:p.Thr77=
NM_012275.3:c.231T>C MANE Select	NP_036407.1:p.Thr77=