Canonical Allele Identifier: CA1280040347
Gene: IL36RN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113062387A= , CM000664.2:g.113062387A= GRCh38
NC_000002.11:g.113819964A= , CM000664.1:g.113819964A= GRCh37
NC_000002.10:g.113536435A= NCBI36
NG_031864.1:g.8750A= , LRG_730:g.8750A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.244-66A= ENSP00000409262.2:n.244-66A=
ENST00000393200.7:c.244-66A= MANE Select ENSP00000376896.2:n.244-66A=
ENST00000346807.7:c.244-66A= ENSP00000259212.3:n.244-66A=
ENST00000393200.6:c.244-66A= ENSP00000376896.2:n.244-66A=
ENST00000437409.1:c.244-66A= ENSP00000409262.1:n.244-66A=
NM_012275.2:c.244-66A= , LRG_730t2:c.244-66A= NP_036407.1:n.244-66A=
NM_173170.1:c.244-66A= , LRG_730t1:c.244-66A= NP_775262.1:n.244-66A=
NM_012275.3:c.244-66A= MANE Select NP_036407.1:n.244-66A=