Canonical Allele Identifier: CA470836185

Gene: CYP2C9

Linked Data

• MyVariant Identifiers: chr10:g.96740947C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94981190C>T , CM000672.2:g.94981190C>T	GRCh38
NC_000010.10:g.96740947C>T , CM000672.1:g.96740947C>T	GRCh37
NC_000010.9:g.96730937C>T	NCBI36
NG_008385.1:g.47533C>T
NG_008385.2:g.48033C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.969C>T MANE Select	ENSP00000260682.6:p.Val323=
ENST00000643112.1:c.827C>T	ENSP00000496202.1:p.Ser276Phe
ENST00000260682.6:c.969C>T	ENSP00000260682.6:p.Val323=
NM_000771.3:c.969C>T	NP_000762.2:p.Val323=
NM_000771.4:c.969C>T MANE Select	NP_000762.2:p.Val323=