Canonical Allele Identifier: CA1280040342
Gene: IL36RN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113062374C= , CM000664.2:g.113062374C= GRCh38
NC_000002.11:g.113819951C= , CM000664.1:g.113819951C= GRCh37
NC_000002.10:g.113536422C= NCBI36
NG_031864.1:g.8737C= , LRG_730:g.8737C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.244-79C= ENSP00000409262.2:n.244-79C=
ENST00000393200.7:c.244-79C= MANE Select ENSP00000376896.2:n.244-79C=
ENST00000346807.7:c.244-79C= ENSP00000259212.3:n.244-79C=
ENST00000393200.6:c.244-79C= ENSP00000376896.2:n.244-79C=
ENST00000437409.1:c.244-79C= ENSP00000409262.1:n.244-79C=
NM_012275.2:c.244-79C= , LRG_730t2:c.244-79C= NP_036407.1:n.244-79C=
NM_173170.1:c.244-79C= , LRG_730t1:c.244-79C= NP_775262.1:n.244-79C=
NM_012275.3:c.244-79C= MANE Select NP_036407.1:n.244-79C=