Canonical Allele Identifier: CA1929341782

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94981138G= , CM000672.2:g.94981138G=	GRCh38
NC_000010.10:g.96740895G= , CM000672.1:g.96740895G=	GRCh37
NC_000010.9:g.96730885G=	NCBI36
NG_008385.1:g.47481G=
NG_008385.2:g.47981G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260682.8:c.962-45G= MANE Select	ENSP00000260682.6:n.962-45G=
ENST00000643112.1:c.820-45G=	ENSP00000496202.1:n.820-45G=
ENST00000260682.6:c.962-45G=	ENSP00000260682.6:n.962-45G=
NM_000771.3:c.962-45G=	NP_000762.2:n.962-45G=
NM_000771.4:c.962-45G= MANE Select	NP_000762.2:n.962-45G=