Canonical Allele Identifier: CA1929340801
Gene: CYP2C59P HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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