Canonical Allele Identifier: CA1838417

Gene: IL36RN

Linked Data

• ClinVar Variation Id: 1652692
• ClinVar RCV Id: RCV002173845
• dbSNP Id: rs749941611
• ExAC: 2:113820019 TCTGC / T
• gnomAD v2: 2-113820019-TCTGC-T
• gnomAD v3: 2-113062442-TCTGC-T
• gnomAD v4: 2-113062442-TCTGC-T
• MyVariant Identifiers: chr2:g.113820020_113820023del (hg19) ; chr2:g.113062443_113062446del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113062444_113062447del , CM000664.2:g.113062444_113062447del	GRCh38
NC_000002.11:g.113820021_113820024del , CM000664.1:g.113820021_113820024del	GRCh37
NC_000002.10:g.113536492_113536495del	NCBI36
NG_031864.1:g.8807_8810del , LRG_730:g.8807_8810del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437409.2:c.244-9_244-6del	ENSP00000409262.2:n.244-9_244-6del
ENST00000393200.7:c.244-9_244-6del MANE Select	ENSP00000376896.2:n.244-9_244-6del
ENST00000346807.7:c.244-9_244-6del	ENSP00000259212.3:n.244-9_244-6del
ENST00000393200.6:c.244-9_244-6del	ENSP00000376896.2:n.244-9_244-6del
ENST00000437409.1:c.244-9_244-6del	ENSP00000409262.1:n.244-9_244-6del
NM_012275.2:c.244-9_244-6del , LRG_730t2:c.244-9_244-6del	NP_036407.1:n.244-9_244-6del
NM_173170.1:c.244-9_244-6del , LRG_730t1:c.244-9_244-6del	NP_775262.1:n.244-9_244-6del
NM_012275.3:c.244-9_244-6del MANE Select	NP_036407.1:n.244-9_244-6del