Canonical Allele Identifier: CA1929292398
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942201T= , CM000672.2:g.94942201T= GRCh38
NC_000010.10:g.96701958T= , CM000672.1:g.96701958T= GRCh37
NC_000010.9:g.96691948T= NCBI36
NG_008385.1:g.8544T=
NG_008385.2:g.9044T=

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.341T= MANE Select ENSP00000260682.6:p.Phe114=
ENST00000643112.1:c.341T= ENSP00000496202.1:p.Phe114=
ENST00000645207.1:n.494T=
ENST00000260682.6:c.341T= ENSP00000260682.6:p.Phe114=
ENST00000461906.1:n.366T=
ENST00000473496.1:n.112T=
NM_000771.3:c.341T= NP_000762.2:p.Phe114=
NM_000771.4:c.341T= MANE Select NP_000762.2:p.Phe114=