Canonical Allele Identifier: CA2779594988

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31033774T>A , CM000670.2:g.31033774T>A	GRCh38
NC_000008.10:g.30891290T>A , CM000670.1:g.30891290T>A	GRCh37
NC_000008.9:g.31010832T>A	NCBI36
NG_008870.1:g.5513T>A , LRG_524:g.5513T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.4:c.-276T>A , LRG_524t1:c.-276T>A	NP_000544.2:n.-276T>A
NM_000553.5:c.-276T>A	NP_000544.2:n.-276T>A
XM_011544639.3:c.-276T>A	XP_011542941.1:n.-276T>A
XR_949470.3:n.26T>A
XR_949471.3:n.26T>A
XR_949472.3:n.26T>A