Canonical Allele Identifier: CA1280039553
Gene: IL36RN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113060891T= , CM000664.2:g.113060891T= GRCh38
NC_000002.11:g.113818468T= , CM000664.1:g.113818468T= GRCh37
NC_000002.10:g.113534939T= NCBI36
NG_031864.1:g.7254T= , LRG_730:g.7254T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.69T= ENSP00000409262.2:p.Asn23=
ENST00000393200.7:c.69T= MANE Select ENSP00000376896.2:p.Asn23=
ENST00000346807.7:c.69T= ENSP00000259212.3:p.Asn23=
ENST00000393200.6:c.69T= ENSP00000376896.2:p.Asn23=
ENST00000437409.1:c.69T= ENSP00000409262.1:p.Asn23=
NM_012275.2:c.69T= , LRG_730t2:c.69T= NP_036407.1:p.Asn23=
NM_173170.1:c.69T= , LRG_730t1:c.69T= NP_775262.1:p.Asn23=
NM_012275.3:c.69T= MANE Select NP_036407.1:p.Asn23=