Canonical Allele Identifier: CA234906711

Gene:

Linked Data

• dbSNP Id: rs922568280
• MyVariant Identifiers: chr12:g.28198128A>C (hg19) ; chr12:g.28045195A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.28045195A>C , CM000674.2:g.28045195A>C	GRCh38
NC_000012.11:g.28198128A>C , CM000674.1:g.28198128A>C	GRCh37
NC_000012.10:g.28089395A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_931460.1:n.154-6237T>G