Canonical Allele Identifier: CA5617433
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs372707224

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989063C>A , CM000672.2:g.94989063C>A GRCh38
NC_000010.10:g.96748820C>A , CM000672.1:g.96748820C>A GRCh37
NC_000010.9:g.96738810C>A NCBI36
NG_008385.1:g.55406C>A
NG_008385.2:g.55906C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.*35C>A MANE Select ENSP00000260682.6:n.*35C>A
ENST00000643112.1:c.*517C>A ENSP00000496202.1:n.*517C>A
ENST00000260682.6:c.*35C>A ENSP00000260682.6:n.*35C>A
NM_000771.3:c.*35C>A NP_000762.2:n.*35C>A
NM_000771.4:c.*35C>A MANE Select NP_000762.2:n.*35C>A