Canonical Allele Identifier: CA470832635

Gene: CYP2C9

Linked Data

• MyVariant Identifiers: chr10:g.96708903G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94949146G>T , CM000672.2:g.94949146G>T	GRCh38
NC_000010.10:g.96708903G>T , CM000672.1:g.96708903G>T	GRCh37
NC_000010.9:g.96698893G>T	NCBI36
NG_008385.1:g.15489G>T
NG_008385.2:g.15989G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.681G>T MANE Select	ENSP00000260682.6:p.Pro227=
ENST00000643112.1:c.681G>T	ENSP00000496202.1:p.Pro227=
ENST00000260682.6:c.681G>T	ENSP00000260682.6:p.Pro227=
ENST00000473496.1:n.452G>T
NM_000771.3:c.681G>T	NP_000762.2:p.Pro227=
NM_000771.4:c.681G>T MANE Select	NP_000762.2:p.Pro227=