Canonical Allele Identifier: CA5617030
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs771237265

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942203A>C , CM000672.2:g.94942203A>C GRCh38
NC_000010.10:g.96701960A>C , CM000672.1:g.96701960A>C GRCh37
NC_000010.9:g.96691950A>C NCBI36
NG_008385.1:g.8546A>C
NG_008385.2:g.9046A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.343A>C MANE Select ENSP00000260682.6:p.Ser115Arg
ENST00000643112.1:c.343A>C ENSP00000496202.1:p.Ser115Arg
ENST00000645207.1:n.496A>C
ENST00000260682.6:c.343A>C ENSP00000260682.6:p.Ser115Arg
ENST00000461906.1:n.368A>C
ENST00000473496.1:n.114A>C
NM_000771.3:c.343A>C NP_000762.2:p.Ser115Arg
NM_000771.4:c.343A>C MANE Select NP_000762.2:p.Ser115Arg