Canonical Allele Identifier: CA377672982
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942200T>G , CM000672.2:g.94942200T>G GRCh38
NC_000010.10:g.96701957T>G , CM000672.1:g.96701957T>G GRCh37
NC_000010.9:g.96691947T>G NCBI36
NG_008385.1:g.8543T>G
NG_008385.2:g.9043T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.340T>G MANE Select ENSP00000260682.6:p.Phe114Val
ENST00000643112.1:c.340T>G ENSP00000496202.1:p.Phe114Val
ENST00000645207.1:n.493T>G
ENST00000260682.6:c.340T>G ENSP00000260682.6:p.Phe114Val
ENST00000461906.1:n.365T>G
ENST00000473496.1:n.111T>G
NM_000771.3:c.340T>G NP_000762.2:p.Phe114Val
NM_000771.4:c.340T>G MANE Select NP_000762.2:p.Phe114Val