Canonical Allele Identifier: CA1838449

Gene: IL36RN

Linked Data

• ClinVar Variation Id: 330780
• ClinVar RCV Id: RCV000275463 ; RCV002263598 ; RCV003912386
• dbSNP Id: rs151274071
• ExAC: 2:113820149 G / A
• gnomAD v2: 2-113820149-G-A
• gnomAD v3: 2-113062572-G-A
• gnomAD v4: 2-113062572-G-A
• MyVariant Identifiers: chr2:g.113820149G>A (hg19) ; chr2:g.113062572G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113062572G>A , CM000664.2:g.113062572G>A	GRCh38
NC_000002.11:g.113820149G>A , CM000664.1:g.113820149G>A	GRCh37
NC_000002.10:g.113536620G>A	NCBI36
NG_031864.1:g.8935G>A , LRG_730:g.8935G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437409.2:c.363G>A	ENSP00000409262.2:p.Leu121=
ENST00000393200.7:c.363G>A MANE Select	ENSP00000376896.2:p.Leu121=
ENST00000346807.7:c.363G>A	ENSP00000259212.3:p.Leu121=
ENST00000393200.6:c.363G>A	ENSP00000376896.2:p.Leu121=
ENST00000514072.1:c.53G>A
NM_012275.2:c.363G>A , LRG_730t2:c.363G>A	NP_036407.1:p.Leu121=
NM_173170.1:c.363G>A , LRG_730t1:c.363G>A	NP_775262.1:p.Leu121=
NM_012275.3:c.363G>A MANE Select	NP_036407.1:p.Leu121=