Canonical Allele Identifier: CA377677078
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988959C>G , CM000672.2:g.94988959C>G GRCh38
NC_000010.10:g.96748716C>G , CM000672.1:g.96748716C>G GRCh37
NC_000010.9:g.96738706C>G NCBI36
NG_008385.1:g.55302C>G
NG_008385.2:g.55802C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1404C>G MANE Select ENSP00000260682.6:p.Asp468Glu
ENST00000643112.1:c.*413C>G ENSP00000496202.1:n.*413C>G
ENST00000260682.6:c.1404C>G ENSP00000260682.6:p.Asp468Glu
NM_000771.3:c.1404C>G NP_000762.2:p.Asp468Glu
NM_000771.4:c.1404C>G MANE Select NP_000762.2:p.Asp468Glu