Canonical Allele Identifier: CA470832640

Gene: CYP2C9

Linked Data

• MyVariant Identifiers: chr10:g.96708909T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94949152T>A , CM000672.2:g.94949152T>A	GRCh38
NC_000010.10:g.96708909T>A , CM000672.1:g.96708909T>A	GRCh37
NC_000010.9:g.96698899T>A	NCBI36
NG_008385.1:g.15495T>A
NG_008385.2:g.15995T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.687T>A MANE Select	ENSP00000260682.6:p.Thr229=
ENST00000643112.1:c.687T>A	ENSP00000496202.1:p.Thr229=
ENST00000260682.6:c.687T>A	ENSP00000260682.6:p.Thr229=
ENST00000473496.1:n.458T>A
NM_000771.3:c.687T>A	NP_000762.2:p.Thr229=
NM_000771.4:c.687T>A MANE Select	NP_000762.2:p.Thr229=