Canonical Allele Identifier: CA377676151
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981198A>G , CM000672.2:g.94981198A>G GRCh38
NC_000010.10:g.96740955A>G , CM000672.1:g.96740955A>G GRCh37
NC_000010.9:g.96730945A>G NCBI36
NG_008385.1:g.47541A>G
NG_008385.2:g.48041A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.977A>G MANE Select ENSP00000260682.6:p.Glu326Gly
ENST00000643112.1:c.835A>G ENSP00000496202.1:p.Arg279Gly
ENST00000260682.6:c.977A>G ENSP00000260682.6:p.Glu326Gly
NM_000771.3:c.977A>G NP_000762.2:p.Glu326Gly
NM_000771.4:c.977A>G MANE Select NP_000762.2:p.Glu326Gly