Canonical Allele Identifier: CA53686992
Gene: IL36RN HGNC NCBI

Linked Data

dbSNP Id: rs867378394

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113060896A>G , CM000664.2:g.113060896A>G GRCh38
NC_000002.11:g.113818473A>G , CM000664.1:g.113818473A>G GRCh37
NC_000002.10:g.113534944A>G NCBI36
NG_031864.1:g.7259A>G , LRG_730:g.7259A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.74A>G ENSP00000409262.2:p.Gln25Arg
ENST00000393200.7:c.74A>G MANE Select ENSP00000376896.2:p.Gln25Arg
ENST00000346807.7:c.74A>G ENSP00000259212.3:p.Gln25Arg
ENST00000393200.6:c.74A>G ENSP00000376896.2:p.Gln25Arg
ENST00000437409.1:c.74A>G ENSP00000409262.1:p.Gln25Arg
NM_012275.2:c.74A>G , LRG_730t2:c.74A>G NP_036407.1:p.Gln25Arg
NM_173170.1:c.74A>G , LRG_730t1:c.74A>G NP_775262.1:p.Gln25Arg
NM_012275.3:c.74A>G MANE Select NP_036407.1:p.Gln25Arg