Canonical Allele Identifier: CA1280039522
Gene: IL36RN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113060811C= , CM000664.2:g.113060811C= GRCh38
NC_000002.11:g.113818388C= , CM000664.1:g.113818388C= GRCh37
NC_000002.10:g.113534859C= NCBI36
NG_031864.1:g.7174C= , LRG_730:g.7174C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.30-41C= ENSP00000409262.2:n.30-41C=
ENST00000393200.7:c.30-41C= MANE Select ENSP00000376896.2:n.30-41C=
ENST00000346807.7:c.30-41C= ENSP00000259212.3:n.30-41C=
ENST00000393200.6:c.30-41C= ENSP00000376896.2:n.30-41C=
ENST00000437409.1:c.30-41C= ENSP00000409262.1:n.30-41C=
NM_012275.2:c.30-41C= , LRG_730t2:c.30-41C= NP_036407.1:n.30-41C=
NM_173170.1:c.30-41C= , LRG_730t1:c.30-41C= NP_775262.1:n.30-41C=
NM_012275.3:c.30-41C= MANE Select NP_036407.1:n.30-41C=