Canonical Allele Identifier: CA1838394
Gene: IL36RN HGNC NCBI

Linked Data

dbSNP Id: rs761173903

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.113062252G>A , CM000664.2:g.113062252G>A GRCh38
NC_000002.11:g.113819829G>A , CM000664.1:g.113819829G>A GRCh37
NC_000002.10:g.113536300G>A NCBI36
NG_031864.1:g.8615G>A , LRG_730:g.8615G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000437409.2:c.243+1G>A ENSP00000409262.2:n.243+1G>A
ENST00000393200.7:c.243+1G>A MANE Select ENSP00000376896.2:n.243+1G>A
ENST00000346807.7:c.243+1G>A ENSP00000259212.3:n.243+1G>A
ENST00000393200.6:c.243+1G>A ENSP00000376896.2:n.243+1G>A
ENST00000437409.1:c.243+1G>A ENSP00000409262.1:n.243+1G>A
NM_012275.2:c.243+1G>A , LRG_730t2:c.243+1G>A NP_036407.1:n.243+1G>A
NM_173170.1:c.243+1G>A , LRG_730t1:c.243+1G>A NP_775262.1:n.243+1G>A
NM_012275.3:c.243+1G>A MANE Select NP_036407.1:n.243+1G>A