Canonical Allele Identifier: CA1929292455
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942313C= , CM000672.2:g.94942313C= GRCh38
NC_000010.10:g.96702070C= , CM000672.1:g.96702070C= GRCh37
NC_000010.9:g.96692060C= NCBI36
NG_008385.1:g.8656C=
NG_008385.2:g.9156C=

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.453C= MANE Select ENSP00000260682.6:p.Cys151=
ENST00000643112.1:c.453C= ENSP00000496202.1:p.Cys151=
ENST00000645207.1:n.606C=
ENST00000260682.6:c.453C= ENSP00000260682.6:p.Cys151=
ENST00000461906.1:n.478C=
ENST00000473496.1:n.224C=
NM_000771.3:c.453C= NP_000762.2:p.Cys151=
NM_000771.4:c.453C= MANE Select NP_000762.2:p.Cys151=