Canonical Allele Identifier: CA5617278
Gene: CYP2C9 HGNC NCBI

Linked Data

ClinVar Variation Id: 370010
dbSNP Id: rs28371685

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981224C>T , CM000672.2:g.94981224C>T GRCh38
NC_000010.10:g.96740981C>T , CM000672.1:g.96740981C>T GRCh37
NC_000010.9:g.96730971C>T NCBI36
NG_008385.1:g.47567C>T
NG_008385.2:g.48067C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1003C>T MANE Select ENSP00000260682.6:p.Arg335Trp
ENST00000643112.1:c.*12C>T ENSP00000496202.1:p.=
ENST00000260682.6:c.1003C>T ENSP00000260682.6:p.Arg335Trp
NM_000771.3:c.1003C>T NP_000762.2:p.Arg335Trp
NM_000771.4:c.1003C>T MANE Select NP_000762.2:p.Arg335Trp