Canonical Allele Identifier: CA470837363

Gene: CYP2C9

Linked Data

• MyVariant Identifiers: chr10:g.96748629C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94988872C>A , CM000672.2:g.94988872C>A	GRCh38
NC_000010.10:g.96748629C>A , CM000672.1:g.96748629C>A	GRCh37
NC_000010.9:g.96738619C>A	NCBI36
NG_008385.1:g.55215C>A
NG_008385.2:g.55715C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.1317C>A MANE Select	ENSP00000260682.6:p.Ala439=
ENST00000643112.1:c.*326C>A	ENSP00000496202.1:n.*326C>A
ENST00000260682.6:c.1317C>A	ENSP00000260682.6:p.Ala439=
NM_000771.3:c.1317C>A	NP_000762.2:p.Ala439=
NM_000771.4:c.1317C>A MANE Select	NP_000762.2:p.Ala439=