Canonical Allele Identifier: CA1929341801

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94981143T= , CM000672.2:g.94981143T=	GRCh38
NC_000010.10:g.96740900T= , CM000672.1:g.96740900T=	GRCh37
NC_000010.9:g.96730890T=	NCBI36
NG_008385.1:g.47486T=
NG_008385.2:g.47986T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260682.8:c.962-40T= MANE Select	ENSP00000260682.6:n.962-40T=
ENST00000643112.1:c.820-40T=	ENSP00000496202.1:n.820-40T=
ENST00000260682.6:c.962-40T=	ENSP00000260682.6:n.962-40T=
NM_000771.3:c.962-40T=	NP_000762.2:n.962-40T=
NM_000771.4:c.962-40T= MANE Select	NP_000762.2:n.962-40T=