Canonical Allele Identifier: CA1929292430

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942268G= , CM000672.2:g.94942268G=	GRCh38
NC_000010.10:g.96702025G= , CM000672.1:g.96702025G=	GRCh37
NC_000010.9:g.96692015G=	NCBI36
NG_008385.1:g.8611G=
NG_008385.2:g.9111G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.408G= MANE Select	ENSP00000260682.6:p.Met136=
ENST00000643112.1:c.408G=	ENSP00000496202.1:p.Met136=
ENST00000645207.1:n.561G=
ENST00000260682.6:c.408G=	ENSP00000260682.6:p.Met136=
ENST00000461906.1:n.433G=
ENST00000473496.1:n.179G=
NM_000771.3:c.408G=	NP_000762.2:p.Met136=
NM_000771.4:c.408G= MANE Select	NP_000762.2:p.Met136=