Canonical Allele Identifier: CA73918678

Gene:

Linked Data

• dbSNP Id: rs944742918
• gnomAD v3: 3-41043909-C-T
• gnomAD v4: 3-41043909-C-T
• MyVariant Identifiers: chr3:g.41085400C>T (hg19) ; chr3:g.41043909C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.41043909C>T , CM000665.2:g.41043909C>T	GRCh38
NC_000003.11:g.41085400C>T , CM000665.1:g.41085400C>T	GRCh37
NC_000003.10:g.41060404C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_940768.1:n.65G>A