Canonical Allele Identifier: CA377677119
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988981T>A , CM000672.2:g.94988981T>A GRCh38
NC_000010.10:g.96748738T>A , CM000672.1:g.96748738T>A GRCh37
NC_000010.9:g.96738728T>A NCBI36
NG_008385.1:g.55324T>A
NG_008385.2:g.55824T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1426T>A MANE Select ENSP00000260682.6:p.Phe476Ile
ENST00000643112.1:c.*435T>A ENSP00000496202.1:n.*435T>A
ENST00000260682.6:c.1426T>A ENSP00000260682.6:p.Phe476Ile
NM_000771.3:c.1426T>A NP_000762.2:p.Phe476Ile
NM_000771.4:c.1426T>A MANE Select NP_000762.2:p.Phe476Ile