Canonical Allele Identifier: CA470987493
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96701959C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942202C>T , CM000672.2:g.94942202C>T GRCh38
NC_000010.10:g.96701959C>T , CM000672.1:g.96701959C>T GRCh37
NC_000010.9:g.96691949C>T NCBI36
NG_008385.1:g.8545C>T
NG_008385.2:g.9045C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.342C>T MANE Select ENSP00000260682.6:p.Phe114=
ENST00000643112.1:c.342C>T ENSP00000496202.1:p.Phe114=
ENST00000645207.1:n.495C>T
ENST00000260682.6:c.342C>T ENSP00000260682.6:p.Phe114=
ENST00000461906.1:n.367C>T
ENST00000473496.1:n.113C>T
NM_000771.3:c.342C>T NP_000762.2:p.Phe114=
NM_000771.4:c.342C>T MANE Select NP_000762.2:p.Phe114=