Canonical Allele Identifier: CA348290175

Gene: IL36RN

Linked Data

• MyVariant Identifiers: chr2:g.113819821C>T (hg19) ; chr2:g.113062244C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113062244C>T , CM000664.2:g.113062244C>T	GRCh38
NC_000002.11:g.113819821C>T , CM000664.1:g.113819821C>T	GRCh37
NC_000002.10:g.113536292C>T	NCBI36
NG_031864.1:g.8607C>T , LRG_730:g.8607C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437409.2:c.236C>T	ENSP00000409262.2:p.Thr79Ile
ENST00000393200.7:c.236C>T MANE Select	ENSP00000376896.2:p.Thr79Ile
ENST00000346807.7:c.236C>T	ENSP00000259212.3:p.Thr79Ile
ENST00000393200.6:c.236C>T	ENSP00000376896.2:p.Thr79Ile
ENST00000437409.1:c.236C>T	ENSP00000409262.1:p.Thr79Ile
NM_012275.2:c.236C>T , LRG_730t2:c.236C>T	NP_036407.1:p.Thr79Ile
NM_173170.1:c.236C>T , LRG_730t1:c.236C>T	NP_775262.1:p.Thr79Ile
NM_012275.3:c.236C>T MANE Select	NP_036407.1:p.Thr79Ile