Canonical Allele Identifier: CA1838465

Gene: IL36RN

Linked Data

• ClinVar Variation Id: 529886
• ClinVar RCV Id: RCV000635395
• dbSNP Id: rs202059991
• ExAC: 2:113820222 A / G
• gnomAD v2: 2-113820222-A-G
• gnomAD v3: 2-113062645-A-G
• gnomAD v4: 2-113062645-A-G
• MyVariant Identifiers: chr2:g.113820222A>G (hg19) ; chr2:g.113062645A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113062645A>G , CM000664.2:g.113062645A>G	GRCh38
NC_000002.11:g.113820222A>G , CM000664.1:g.113820222A>G	GRCh37
NC_000002.10:g.113536693A>G	NCBI36
NG_031864.1:g.9008A>G , LRG_730:g.9008A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000437409.2:c.436A>G	ENSP00000409262.2:p.Ile146Val
ENST00000393200.7:c.436A>G MANE Select	ENSP00000376896.2:p.Ile146Val
ENST00000346807.7:c.436A>G	ENSP00000259212.3:p.Ile146Val
ENST00000393200.6:c.436A>G	ENSP00000376896.2:p.Ile146Val
ENST00000514072.1:c.126A>G
NM_012275.2:c.436A>G , LRG_730t2:c.436A>G	NP_036407.1:p.Ile146Val
NM_173170.1:c.436A>G , LRG_730t1:c.436A>G	NP_775262.1:p.Ile146Val
NM_012275.3:c.436A>G MANE Select	NP_036407.1:p.Ile146Val