Canonical Allele Identifier: CA2660759428
Gene: IL36RN HGNC NCBI

Linked Data

dbSNP Id: rs2105069603

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113062396A>C , CM000664.2:g.113062396A>C GRCh38
NC_000002.11:g.113819973A>C , CM000664.1:g.113819973A>C GRCh37
NC_000002.10:g.113536444A>C NCBI36
NG_031864.1:g.8759A>C , LRG_730:g.8759A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.244-57A>C ENSP00000409262.2:n.244-57A>C
ENST00000393200.7:c.244-57A>C MANE Select ENSP00000376896.2:n.244-57A>C
ENST00000346807.7:c.244-57A>C ENSP00000259212.3:n.244-57A>C
ENST00000393200.6:c.244-57A>C ENSP00000376896.2:n.244-57A>C
ENST00000437409.1:c.244-57A>C ENSP00000409262.1:n.244-57A>C
NM_012275.2:c.244-57A>C , LRG_730t2:c.244-57A>C NP_036407.1:n.244-57A>C
NM_173170.1:c.244-57A>C , LRG_730t1:c.244-57A>C NP_775262.1:n.244-57A>C
NM_012275.3:c.244-57A>C MANE Select NP_036407.1:n.244-57A>C