Canonical Allele Identifier: CA1929292461
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942321A= , CM000672.2:g.94942321A= GRCh38
NC_000010.10:g.96702078A= , CM000672.1:g.96702078A= GRCh37
NC_000010.9:g.96692068A= NCBI36
NG_008385.1:g.8664A=
NG_008385.2:g.9164A=

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.461A= MANE Select ENSP00000260682.6:p.Glu154=
ENST00000643112.1:c.461A= ENSP00000496202.1:p.Glu154=
ENST00000645207.1:n.614A=
ENST00000260682.6:c.461A= ENSP00000260682.6:p.Glu154=
ENST00000461906.1:n.486A=
ENST00000473496.1:n.232A=
NM_000771.3:c.461A= NP_000762.2:p.Glu154=
NM_000771.4:c.461A= MANE Select NP_000762.2:p.Glu154=