Canonical Allele Identifier: CA535596122

Gene: IL36RN

Linked Data

• dbSNP Id: rs1287159370
• gnomAD v2: 2-113819869-T-C
• gnomAD v4: 2-113062292-T-C
• MyVariant Identifiers: chr2:g.113819869T>C (hg19) ; chr2:g.113062292T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.113062292T>C , CM000664.2:g.113062292T>C	GRCh38
NC_000002.11:g.113819869T>C , CM000664.1:g.113819869T>C	GRCh37
NC_000002.10:g.113536340T>C	NCBI36
NG_031864.1:g.8655T>C , LRG_730:g.8655T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437409.2:c.243+41T>C	ENSP00000409262.2:n.243+41T>C
ENST00000393200.7:c.243+41T>C MANE Select	ENSP00000376896.2:n.243+41T>C
ENST00000346807.7:c.243+41T>C	ENSP00000259212.3:n.243+41T>C
ENST00000393200.6:c.243+41T>C	ENSP00000376896.2:n.243+41T>C
ENST00000437409.1:c.243+41T>C	ENSP00000409262.1:n.243+41T>C
NM_012275.2:c.243+41T>C , LRG_730t2:c.243+41T>C	NP_036407.1:n.243+41T>C
NM_173170.1:c.243+41T>C , LRG_730t1:c.243+41T>C	NP_775262.1:n.243+41T>C
NM_012275.3:c.243+41T>C MANE Select	NP_036407.1:n.243+41T>C