Canonical Allele Identifier: CA234906703

Gene:

Linked Data

• dbSNP Id: rs141369668
• gnomAD v2: 12-28197998-C-A
• gnomAD v3: 12-28045065-C-A
• gnomAD v4: 12-28045065-C-A
• MyVariant Identifiers: chr12:g.28197998C>A (hg19) ; chr12:g.28045065C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.28045065C>A , CM000674.2:g.28045065C>A	GRCh38
NC_000012.11:g.28197998C>A , CM000674.1:g.28197998C>A	GRCh37
NC_000012.10:g.28089265C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_931460.1:n.154-6107G>T