Canonical Allele Identifier: CA850706357

Gene: WRN

Linked Data

• dbSNP Id: rs369873912
• MyVariant Identifiers: chr8:g.30891302T>A (hg19) ; chr8:g.31033786T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31033786T>A , CM000670.2:g.31033786T>A	GRCh38
NC_000008.10:g.30891302T>A , CM000670.1:g.30891302T>A	GRCh37
NC_000008.9:g.31010844T>A	NCBI36
NG_008870.1:g.5525T>A , LRG_524:g.5525T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.4:c.-264T>A , LRG_524t1:c.-264T>A	NP_000544.2:n.-264T>A
XM_011544639.1:c.-264T>A	XP_011542941.1:n.-264T>A
XR_949470.1:n.10T>A
XR_949471.1:n.10T>A
XR_949472.1:n.10T>A
NM_000553.5:c.-264T>A	NP_000544.2:n.-264T>A
XM_011544639.3:c.-264T>A	XP_011542941.1:n.-264T>A
XM_024447265.1:c.-598T>A	XP_024303033.1:n.-598T>A
XR_949470.3:n.38T>A
XR_949471.3:n.38T>A
XR_949472.3:n.38T>A