Canonical Allele Identifier: CA1929292405
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942217A= , CM000672.2:g.94942217A= GRCh38
NC_000010.10:g.96701974A= , CM000672.1:g.96701974A= GRCh37
NC_000010.9:g.96691964A= NCBI36
NG_008385.1:g.8560A=
NG_008385.2:g.9060A=

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.357A= MANE Select ENSP00000260682.6:p.Lys119=
ENST00000643112.1:c.357A= ENSP00000496202.1:p.Lys119=
ENST00000645207.1:n.510A=
ENST00000260682.6:c.357A= ENSP00000260682.6:p.Lys119=
ENST00000461906.1:n.382A=
ENST00000473496.1:n.128A=
NM_000771.3:c.357A= NP_000762.2:p.Lys119=
NM_000771.4:c.357A= MANE Select NP_000762.2:p.Lys119=