Canonical Allele Identifier: CA377673025
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942218T>A , CM000672.2:g.94942218T>A GRCh38
NC_000010.10:g.96701975T>A , CM000672.1:g.96701975T>A GRCh37
NC_000010.9:g.96691965T>A NCBI36
NG_008385.1:g.8561T>A
NG_008385.2:g.9061T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.358T>A MANE Select ENSP00000260682.6:p.Trp120Arg
ENST00000643112.1:c.358T>A ENSP00000496202.1:p.Trp120Arg
ENST00000645207.1:n.511T>A
ENST00000260682.6:c.358T>A ENSP00000260682.6:p.Trp120Arg
ENST00000461906.1:n.383T>A
ENST00000473496.1:n.129T>A
NM_000771.3:c.358T>A NP_000762.2:p.Trp120Arg
NM_000771.4:c.358T>A MANE Select NP_000762.2:p.Trp120Arg