Canonical Allele Identifier: CA234906710

Gene:

Linked Data

• dbSNP Id: rs976799866
• MyVariant Identifiers: chr12:g.28198094T>C (hg19) ; chr12:g.28045161T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.28045161T>C , CM000674.2:g.28045161T>C	GRCh38
NC_000012.11:g.28198094T>C , CM000674.1:g.28198094T>C	GRCh37
NC_000012.10:g.28089361T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_931460.1:n.154-6203A>G