Canonical Allele Identifier: CA1838452

Gene: IL36RN

Linked Data

• ClinVar Variation Id: 529888
• ClinVar RCV Id: RCV000635397 ; RCV002263870
• dbSNP Id: rs28938778
• ExAC: 2:113820155 G / C
• gnomAD v2: 2-113820155-G-C
• gnomAD v3: 2-113062578-G-C
• gnomAD v4: 2-113062578-G-C
• MyVariant Identifiers: chr2:g.113820155G>C (hg19) ; chr2:g.113062578G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113062578G>C , CM000664.2:g.113062578G>C	GRCh38
NC_000002.11:g.113820155G>C , CM000664.1:g.113820155G>C	GRCh37
NC_000002.10:g.113536626G>C	NCBI36
NG_031864.1:g.8941G>C , LRG_730:g.8941G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437409.2:c.369G>C	ENSP00000409262.2:p.Thr123=
ENST00000393200.7:c.369G>C MANE Select	ENSP00000376896.2:p.Thr123=
ENST00000346807.7:c.369G>C	ENSP00000259212.3:p.Thr123=
ENST00000393200.6:c.369G>C	ENSP00000376896.2:p.Thr123=
ENST00000514072.1:c.59G>C
NM_012275.2:c.369G>C , LRG_730t2:c.369G>C	NP_036407.1:p.Thr123=
NM_173170.1:c.369G>C , LRG_730t1:c.369G>C	NP_775262.1:p.Thr123=
NM_012275.3:c.369G>C MANE Select	NP_036407.1:p.Thr123=