Canonical Allele Identifier: CA1035134214
Gene: IL36RN HGNC NCBI

Linked Data

dbSNP Id: rs1685662358

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113062470del , CM000664.2:g.113062470del GRCh38
NC_000002.11:g.113820047del , CM000664.1:g.113820047del GRCh37
NC_000002.10:g.113536518del NCBI36
NG_031864.1:g.8833del , LRG_730:g.8833del

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.261del ENSP00000409262.2:p.Glu87AspfsTer?
ENST00000393200.7:c.261del MANE Select ENSP00000376896.2:p.Glu87AspfsTer?
ENST00000346807.7:c.261del ENSP00000259212.3:p.Glu87AspfsTer?
ENST00000393200.6:c.261del ENSP00000376896.2:p.Glu87AspfsTer?
ENST00000437409.1:c.261del ENSP00000409262.1:p.Glu87AspfsTer?
NM_012275.2:c.261del , LRG_730t2:c.261del NP_036407.1:p.Glu87AspfsTer?
NM_173170.1:c.261del , LRG_730t1:c.261del NP_775262.1:p.Glu87AspfsTer?
NM_012275.3:c.261del MANE Select NP_036407.1:p.Glu87AspfsTer?