Canonical Allele Identifier: CA692802515

Gene:

Linked Data

• dbSNP Id: rs1263102236
• MyVariant Identifiers: chr12:g.85345749A>T (hg19) ; chr12:g.84951970A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.84951970A>T , CM000674.2:g.84951970A>T	GRCh38
NC_000012.11:g.85345749A>T , CM000674.1:g.85345749A>T	GRCh37
NC_000012.10:g.83869880A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945152.1:n.316+30656A>T
XR_945153.1:n.301+13506A>T
XR_945154.1:n.175-36972A>T
XR_945155.1:n.330+30656A>T
XR_945152.2:n.316+30656A>T
XR_945154.2:n.175-36972A>T
XR_945155.2:n.888+30656A>T