Canonical Allele Identifier: CA470837937

Gene: CYP2C59P

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95007177A>T , CM000672.2:g.95007177A>T	GRCh38
NC_000010.10:g.96766934A>T , CM000672.1:g.96766934A>T	GRCh37
NC_000010.9:g.96756924A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457790.1:n.218T>A