Canonical Allele Identifier: CA174888543

Gene: WRN

Linked Data

• dbSNP Id: rs957211401
• gnomAD v3: 8-31033745-T-G
• gnomAD v4: 8-31033745-T-G
• MyVariant Identifiers: chr8:g.30891261T>G (hg19) ; chr8:g.31033745T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31033745T>G , CM000670.2:g.31033745T>G	GRCh38
NC_000008.10:g.30891261T>G , CM000670.1:g.30891261T>G	GRCh37
NC_000008.9:g.31010803T>G	NCBI36
NG_008870.1:g.5484T>G , LRG_524:g.5484T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.4:c.-305T>G , LRG_524t1:c.-305T>G	NP_000544.2:n.-305T>G
NM_000553.5:c.-305T>G	NP_000544.2:n.-305T>G