Canonical Allele Identifier: CA580974729

Gene: WRN

Linked Data

• dbSNP Id: rs1377606866
• gnomAD v2: 8-30891310-G-A
• gnomAD v3: 8-31033794-G-A
• gnomAD v4: 8-31033794-G-A
• MyVariant Identifiers: chr8:g.30891310G>A (hg19) ; chr8:g.31033794G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31033794G>A , CM000670.2:g.31033794G>A	GRCh38
NC_000008.10:g.30891310G>A , CM000670.1:g.30891310G>A	GRCh37
NC_000008.9:g.31010852G>A	NCBI36
NG_008870.1:g.5533G>A , LRG_524:g.5533G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650667.1:c.-256G>A	ENSP00000498593.1:n.-256G>A
NM_000553.4:c.-256G>A , LRG_524t1:c.-256G>A	NP_000544.2:n.-256G>A
XM_011544639.1:c.-256G>A	XP_011542941.1:n.-256G>A
XR_949470.1:n.18G>A
XR_949471.1:n.18G>A
XR_949472.1:n.18G>A
NM_000553.5:c.-256G>A	NP_000544.2:n.-256G>A
XM_011544639.3:c.-256G>A	XP_011542941.1:n.-256G>A
XM_024447265.1:c.-590G>A	XP_024303033.1:n.-590G>A
XR_949470.3:n.46G>A
XR_949471.3:n.46G>A
XR_949472.3:n.46G>A