Canonical Allele Identifier: CA1929292458
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.458T= MANE Select ENSP00000260682.6:p.Val153=
ENST00000643112.1:c.458T= ENSP00000496202.1:p.Val153=
ENST00000645207.1:n.611T=
ENST00000260682.6:c.458T= ENSP00000260682.6:p.Val153=
ENST00000461906.1:n.483T=
ENST00000473496.1:n.229T=
NM_000771.3:c.458T= NP_000762.2:p.Val153=
NM_000771.4:c.458T= MANE Select NP_000762.2:p.Val153=