Canonical Allele Identifier: CA377677144
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs530950257

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988994C>G , CM000672.2:g.94988994C>G GRCh38
NC_000010.10:g.96748751C>G , CM000672.1:g.96748751C>G GRCh37
NC_000010.9:g.96738741C>G NCBI36
NG_008385.1:g.55337C>G
NG_008385.2:g.55837C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1439C>G MANE Select ENSP00000260682.6:p.Pro480Arg
ENST00000643112.1:c.*448C>G ENSP00000496202.1:n.*448C>G
ENST00000260682.6:c.1439C>G ENSP00000260682.6:p.Pro480Arg
NM_000771.3:c.1439C>G NP_000762.2:p.Pro480Arg
NM_000771.4:c.1439C>G MANE Select NP_000762.2:p.Pro480Arg