Canonical Allele Identifier: CA580974728

Gene: WRN

Linked Data

• gnomAD v2: 8-30891308-A-T
• MyVariant Identifiers: chr8:g.30891308A>T (hg19) ; chr8:g.31033792A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31033792A>T , CM000670.2:g.31033792A>T	GRCh38
NC_000008.10:g.30891308A>T , CM000670.1:g.30891308A>T	GRCh37
NC_000008.9:g.31010850A>T	NCBI36
NG_008870.1:g.5531A>T , LRG_524:g.5531A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650667.1:c.-258A>T	ENSP00000498593.1:n.-258A>T
NM_000553.4:c.-258A>T , LRG_524t1:c.-258A>T	NP_000544.2:n.-258A>T
XM_011544639.1:c.-258A>T	XP_011542941.1:n.-258A>T
XR_949470.1:n.16A>T
XR_949471.1:n.16A>T
XR_949472.1:n.16A>T
NM_000553.5:c.-258A>T	NP_000544.2:n.-258A>T
XM_011544639.3:c.-258A>T	XP_011542941.1:n.-258A>T
XM_024447265.1:c.-592A>T	XP_024303033.1:n.-592A>T
XR_949470.3:n.44A>T
XR_949471.3:n.44A>T
XR_949472.3:n.44A>T