Canonical Allele Identifier: CA377676997
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988922T>A , CM000672.2:g.94988922T>A GRCh38
NC_000010.10:g.96748679T>A , CM000672.1:g.96748679T>A GRCh37
NC_000010.9:g.96738669T>A NCBI36
NG_008385.1:g.55265T>A
NG_008385.2:g.55765T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1367T>A MANE Select ENSP00000260682.6:p.Phe456Tyr
ENST00000643112.1:c.*376T>A ENSP00000496202.1:n.*376T>A
ENST00000260682.6:c.1367T>A ENSP00000260682.6:p.Phe456Tyr
NM_000771.3:c.1367T>A NP_000762.2:p.Phe456Tyr
NM_000771.4:c.1367T>A MANE Select NP_000762.2:p.Phe456Tyr