Canonical Allele Identifier: CA1929341780

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94981136G= , CM000672.2:g.94981136G=	GRCh38
NC_000010.10:g.96740893G= , CM000672.1:g.96740893G=	GRCh37
NC_000010.9:g.96730883G=	NCBI36
NG_008385.1:g.47479G=
NG_008385.2:g.47979G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260682.8:c.962-47G= MANE Select	ENSP00000260682.6:n.962-47G=
ENST00000643112.1:c.820-47G=	ENSP00000496202.1:n.820-47G=
ENST00000260682.6:c.962-47G=	ENSP00000260682.6:n.962-47G=
NM_000771.3:c.962-47G=	NP_000762.2:n.962-47G=
NM_000771.4:c.962-47G= MANE Select	NP_000762.2:n.962-47G=