Canonical Allele Identifier: CA1929292253
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942001A= , CM000672.2:g.94942001A= GRCh38
NC_000010.10:g.96701758A= , CM000672.1:g.96701758A= GRCh37
NC_000010.9:g.96691748A= NCBI36
NG_008385.1:g.8344A=
NG_008385.2:g.8844A=

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.312A= MANE Select ENSP00000260682.6:p.Glu104=
ENST00000643112.1:c.312A= ENSP00000496202.1:p.Glu104=
ENST00000645207.1:n.465A=
ENST00000260682.6:c.312A= ENSP00000260682.6:p.Glu104=
ENST00000461906.1:n.337A=
ENST00000473496.1:n.83A=
NM_000771.3:c.312A= NP_000762.2:p.Glu104=
NM_000771.4:c.312A= MANE Select NP_000762.2:p.Glu104=