Canonical Allele Identifier: CA377676145
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981196A>T , CM000672.2:g.94981196A>T GRCh38
NC_000010.10:g.96740953A>T , CM000672.1:g.96740953A>T GRCh37
NC_000010.9:g.96730943A>T NCBI36
NG_008385.1:g.47539A>T
NG_008385.2:g.48039A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.975A>T MANE Select ENSP00000260682.6:p.Glu325Asp
ENST00000643112.1:c.833A>T ENSP00000496202.1:p.Lys278Met
ENST00000260682.6:c.975A>T ENSP00000260682.6:p.Glu325Asp
NM_000771.3:c.975A>T NP_000762.2:p.Glu325Asp
NM_000771.4:c.975A>T MANE Select NP_000762.2:p.Glu325Asp