Canonical Allele Identifier: CA377672837

Gene: CYP2C9

Linked Data

• MyVariant Identifiers: chr10:g.96701720G>A (hg19) ; chr10:g.94941963G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94941963G>A , CM000672.2:g.94941963G>A	GRCh38
NC_000010.10:g.96701720G>A , CM000672.1:g.96701720G>A	GRCh37
NC_000010.9:g.96691710G>A	NCBI36
NG_008385.1:g.8306G>A
NG_008385.2:g.8806G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.274G>A MANE Select	ENSP00000260682.6:p.Glu92Lys
ENST00000643112.1:c.274G>A	ENSP00000496202.1:p.Glu92Lys
ENST00000645207.1:n.427G>A
ENST00000260682.6:c.274G>A	ENSP00000260682.6:p.Glu92Lys
ENST00000461906.1:n.299G>A
ENST00000473496.1:n.45G>A
NM_000771.3:c.274G>A	NP_000762.2:p.Glu92Lys
NM_000771.4:c.274G>A MANE Select	NP_000762.2:p.Glu92Lys