Canonical Allele Identifier: CA1929292260

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942022T= , CM000672.2:g.94942022T=	GRCh38
NC_000010.10:g.96701779T= , CM000672.1:g.96701779T=	GRCh37
NC_000010.9:g.96691769T=	NCBI36
NG_008385.1:g.8365T=
NG_008385.2:g.8865T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260682.8:c.331+2T= MANE Select	ENSP00000260682.6:n.331+2T=
ENST00000643112.1:c.331+2T=	ENSP00000496202.1:n.331+2T=
ENST00000645207.1:n.484+2T=
ENST00000260682.6:c.331+2T=	ENSP00000260682.6:n.331+2T=
ENST00000461906.1:n.356+2T=
ENST00000473496.1:n.102+2T=
NM_000771.3:c.331+2T=	NP_000762.2:n.331+2T=
NM_000771.4:c.331+2T= MANE Select	NP_000762.2:n.331+2T=