Canonical Allele Identifier: CA377677066
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988953C>G , CM000672.2:g.94988953C>G GRCh38
NC_000010.10:g.96748710C>G , CM000672.1:g.96748710C>G GRCh37
NC_000010.9:g.96738700C>G NCBI36
NG_008385.1:g.55296C>G
NG_008385.2:g.55796C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1398C>G MANE Select ENSP00000260682.6:p.Asn466Lys
ENST00000643112.1:c.*407C>G ENSP00000496202.1:n.*407C>G
ENST00000260682.6:c.1398C>G ENSP00000260682.6:p.Asn466Lys
NM_000771.3:c.1398C>G NP_000762.2:p.Asn466Lys
NM_000771.4:c.1398C>G MANE Select NP_000762.2:p.Asn466Lys