Canonical Allele Identifier: CA377676945
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988897T>A , CM000672.2:g.94988897T>A GRCh38
NC_000010.10:g.96748654T>A , CM000672.1:g.96748654T>A GRCh37
NC_000010.9:g.96738644T>A NCBI36
NG_008385.1:g.55240T>A
NG_008385.2:g.55740T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1342T>A MANE Select ENSP00000260682.6:p.Phe448Ile
ENST00000643112.1:c.*351T>A ENSP00000496202.1:n.*351T>A
ENST00000260682.6:c.1342T>A ENSP00000260682.6:p.Phe448Ile
NM_000771.3:c.1342T>A NP_000762.2:p.Phe448Ile
NM_000771.4:c.1342T>A MANE Select NP_000762.2:p.Phe448Ile