Canonical Allele Identifier: CA1280039556
Gene: IL36RN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113060897G= , CM000664.2:g.113060897G= GRCh38
NC_000002.11:g.113818474G= , CM000664.1:g.113818474G= GRCh37
NC_000002.10:g.113534945G= NCBI36
NG_031864.1:g.7260G= , LRG_730:g.7260G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.75G= ENSP00000409262.2:p.Gln25=
ENST00000393200.7:c.75G= MANE Select ENSP00000376896.2:p.Gln25=
ENST00000346807.7:c.75G= ENSP00000259212.3:p.Gln25=
ENST00000393200.6:c.75G= ENSP00000376896.2:p.Gln25=
ENST00000437409.1:c.75G= ENSP00000409262.1:p.Gln25=
NM_012275.2:c.75G= , LRG_730t2:c.75G= NP_036407.1:p.Gln25=
NM_173170.1:c.75G= , LRG_730t1:c.75G= NP_775262.1:p.Gln25=
NM_012275.3:c.75G= MANE Select NP_036407.1:p.Gln25=