Canonical Allele Identifier: CA1838404
Gene: IL36RN HGNC NCBI

Linked Data

dbSNP Id: rs778758453

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113062411_113062412dup , CM000664.2:g.113062411_113062412dup GRCh38
NC_000002.11:g.113819988_113819989dup , CM000664.1:g.113819988_113819989dup GRCh37
NC_000002.10:g.113536459_113536460dup NCBI36
NG_031864.1:g.8774_8775dup , LRG_730:g.8774_8775dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.244-42_244-41dup ENSP00000409262.2:n.244-42_244-41dup
ENST00000393200.7:c.244-42_244-41dup MANE Select ENSP00000376896.2:n.244-42_244-41dup
ENST00000346807.7:c.244-42_244-41dup ENSP00000259212.3:n.244-42_244-41dup
ENST00000393200.6:c.244-42_244-41dup ENSP00000376896.2:n.244-42_244-41dup
ENST00000437409.1:c.244-42_244-41dup ENSP00000409262.1:n.244-42_244-41dup
NM_012275.2:c.244-42_244-41dup , LRG_730t2:c.244-42_244-41dup NP_036407.1:n.244-42_244-41dup
NM_173170.1:c.244-42_244-41dup , LRG_730t1:c.244-42_244-41dup NP_775262.1:n.244-42_244-41dup
NM_012275.3:c.244-42_244-41dup MANE Select NP_036407.1:n.244-42_244-41dup