Canonical Allele Identifier: CA1929292249

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94941992A= , CM000672.2:g.94941992A=	GRCh38
NC_000010.10:g.96701749A= , CM000672.1:g.96701749A=	GRCh37
NC_000010.9:g.96691739A=	NCBI36
NG_008385.1:g.8335A=
NG_008385.2:g.8835A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.303A= MANE Select	ENSP00000260682.6:p.Pro101=
ENST00000643112.1:c.303A=	ENSP00000496202.1:p.Pro101=
ENST00000645207.1:n.456A=
ENST00000260682.6:c.303A=	ENSP00000260682.6:p.Pro101=
ENST00000461906.1:n.328A=
ENST00000473496.1:n.74A=
NM_000771.3:c.303A=	NP_000762.2:p.Pro101=
NM_000771.4:c.303A= MANE Select	NP_000762.2:p.Pro101=