Canonical Allele Identifier: CA1929349811

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94988977T= , CM000672.2:g.94988977T=	GRCh38
NC_000010.10:g.96748734T= , CM000672.1:g.96748734T=	GRCh37
NC_000010.9:g.96738724T=	NCBI36
NG_008385.1:g.55320T=
NG_008385.2:g.55820T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260682.8:c.1422T= MANE Select	ENSP00000260682.6:p.Asn474=
ENST00000643112.1:c.*431T=	ENSP00000496202.1:n.*431T=
ENST00000260682.6:c.1422T=	ENSP00000260682.6:p.Asn474=
NM_000771.3:c.1422T=	NP_000762.2:p.Asn474=
NM_000771.4:c.1422T= MANE Select	NP_000762.2:p.Asn474=