Canonical Allele Identifier: CA5617385
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs761946333

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988854G>A , CM000672.2:g.94988854G>A GRCh38
NC_000010.10:g.96748611G>A , CM000672.1:g.96748611G>A GRCh37
NC_000010.9:g.96738601G>A NCBI36
NG_008385.1:g.55197G>A
NG_008385.2:g.55697G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1299G>A MANE Select ENSP00000260682.6:p.Arg433=
ENST00000643112.1:c.*308G>A ENSP00000496202.1:n.*308G>A
ENST00000260682.6:c.1299G>A ENSP00000260682.6:p.Arg433=
NM_000771.3:c.1299G>A NP_000762.2:p.Arg433=
NM_000771.4:c.1299G>A MANE Select NP_000762.2:p.Arg433=