Canonical Allele Identifier: CA348290035
Gene: IL36RN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113062174C>T , CM000664.2:g.113062174C>T GRCh38
NC_000002.11:g.113819751C>T , CM000664.1:g.113819751C>T GRCh37
NC_000002.10:g.113536222C>T NCBI36
NG_031864.1:g.8537C>T , LRG_730:g.8537C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.166C>T ENSP00000409262.2:p.Pro56Ser
ENST00000393200.7:c.166C>T MANE Select ENSP00000376896.2:p.Pro56Ser
ENST00000346807.7:c.166C>T ENSP00000259212.3:p.Pro56Ser
ENST00000393200.6:c.166C>T ENSP00000376896.2:p.Pro56Ser
ENST00000437409.1:c.166C>T ENSP00000409262.1:p.Pro56Ser
NM_012275.2:c.166C>T , LRG_730t2:c.166C>T NP_036407.1:p.Pro56Ser
NM_173170.1:c.166C>T , LRG_730t1:c.166C>T NP_775262.1:p.Pro56Ser
NM_012275.3:c.166C>T MANE Select NP_036407.1:p.Pro56Ser