Canonical Allele Identifier: CA377673360
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942323G>A , CM000672.2:g.94942323G>A GRCh38
NC_000010.10:g.96702080G>A , CM000672.1:g.96702080G>A GRCh37
NC_000010.9:g.96692070G>A NCBI36
NG_008385.1:g.8666G>A
NG_008385.2:g.9166G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.463G>A MANE Select ENSP00000260682.6:p.Glu155Lys
ENST00000643112.1:c.463G>A ENSP00000496202.1:p.Glu155Lys
ENST00000645207.1:n.616G>A
ENST00000260682.6:c.463G>A ENSP00000260682.6:p.Glu155Lys
ENST00000461906.1:n.488G>A
ENST00000473496.1:n.234G>A
NM_000771.3:c.463G>A NP_000762.2:p.Glu155Lys
NM_000771.4:c.463G>A MANE Select NP_000762.2:p.Glu155Lys