Canonical Allele Identifier: CA234906709

Gene:

Linked Data

• dbSNP Id: rs558800034
• MyVariant Identifiers: chr12:g.28198077G>A (hg19) ; chr12:g.28045144G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.28045144G>A , CM000674.2:g.28045144G>A	GRCh38
NC_000012.11:g.28198077G>A , CM000674.1:g.28198077G>A	GRCh37
NC_000012.10:g.28089344G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_931460.1:n.154-6186C>T