Canonical Allele Identifier: CA1929349813
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988978G= , CM000672.2:g.94988978G= GRCh38
NC_000010.10:g.96748735G= , CM000672.1:g.96748735G= GRCh37
NC_000010.9:g.96738725G= NCBI36
NG_008385.1:g.55321G=
NG_008385.2:g.55821G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1423G= MANE Select ENSP00000260682.6:p.Gly475=
ENST00000643112.1:c.*432G= ENSP00000496202.1:n.*432G=
ENST00000260682.6:c.1423G= ENSP00000260682.6:p.Gly475=
NM_000771.3:c.1423G= NP_000762.2:p.Gly475=
NM_000771.4:c.1423G= MANE Select NP_000762.2:p.Gly475=