Canonical Allele Identifier: CA850706351

Gene: WRN

Linked Data

• dbSNP Id: rs1309189592
• gnomAD v3: 8-31033782-C-G
• gnomAD v4: 8-31033782-C-G
• MyVariant Identifiers: chr8:g.30891298C>G (hg19) ; chr8:g.31033782C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31033782C>G , CM000670.2:g.31033782C>G	GRCh38
NC_000008.10:g.30891298C>G , CM000670.1:g.30891298C>G	GRCh37
NC_000008.9:g.31010840C>G	NCBI36
NG_008870.1:g.5521C>G , LRG_524:g.5521C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.4:c.-268C>G , LRG_524t1:c.-268C>G	NP_000544.2:n.-268C>G
XM_011544639.1:c.-268C>G	XP_011542941.1:n.-268C>G
XR_949470.1:n.6C>G
XR_949471.1:n.6C>G
XR_949472.1:n.6C>G
NM_000553.5:c.-268C>G	NP_000544.2:n.-268C>G
XM_011544639.3:c.-268C>G	XP_011542941.1:n.-268C>G
XM_024447265.1:c.-602C>G	XP_024303033.1:n.-602C>G
XR_949470.3:n.34C>G
XR_949471.3:n.34C>G
XR_949472.3:n.34C>G