Canonical Allele Identifier: CA348290077
Gene: IL36RN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113062196G>A , CM000664.2:g.113062196G>A GRCh38
NC_000002.11:g.113819773G>A , CM000664.1:g.113819773G>A GRCh37
NC_000002.10:g.113536244G>A NCBI36
NG_031864.1:g.8559G>A , LRG_730:g.8559G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.188G>A ENSP00000409262.2:p.Gly63Asp
ENST00000393200.7:c.188G>A MANE Select ENSP00000376896.2:p.Gly63Asp
ENST00000346807.7:c.188G>A ENSP00000259212.3:p.Gly63Asp
ENST00000393200.6:c.188G>A ENSP00000376896.2:p.Gly63Asp
ENST00000437409.1:c.188G>A ENSP00000409262.1:p.Gly63Asp
NM_012275.2:c.188G>A , LRG_730t2:c.188G>A NP_036407.1:p.Gly63Asp
NM_173170.1:c.188G>A , LRG_730t1:c.188G>A NP_775262.1:p.Gly63Asp
NM_012275.3:c.188G>A MANE Select NP_036407.1:p.Gly63Asp