Canonical Allele Identifier: CA377673339
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942318T>A , CM000672.2:g.94942318T>A GRCh38
NC_000010.10:g.96702075T>A , CM000672.1:g.96702075T>A GRCh37
NC_000010.9:g.96692065T>A NCBI36
NG_008385.1:g.8661T>A
NG_008385.2:g.9161T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.458T>A MANE Select ENSP00000260682.6:p.Val153Glu
ENST00000643112.1:c.458T>A ENSP00000496202.1:p.Val153Glu
ENST00000645207.1:n.611T>A
ENST00000260682.6:c.458T>A ENSP00000260682.6:p.Val153Glu
ENST00000461906.1:n.483T>A
ENST00000473496.1:n.229T>A
NM_000771.3:c.458T>A NP_000762.2:p.Val153Glu
NM_000771.4:c.458T>A MANE Select NP_000762.2:p.Val153Glu