Canonical Allele Identifier: CA377673045

Gene: CYP2C9

Linked Data

• gnomAD v4: 10-94942225-A-T
• MyVariant Identifiers: chr10:g.96701982A>T (hg19) ; chr10:g.94942225A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942225A>T , CM000672.2:g.94942225A>T	GRCh38
NC_000010.10:g.96701982A>T , CM000672.1:g.96701982A>T	GRCh37
NC_000010.9:g.96691972A>T	NCBI36
NG_008385.1:g.8568A>T
NG_008385.2:g.9068A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260682.8:c.365A>T MANE Select	ENSP00000260682.6:p.Glu122Val
ENST00000643112.1:c.365A>T	ENSP00000496202.1:p.Glu122Val
ENST00000645207.1:n.518A>T
ENST00000260682.6:c.365A>T	ENSP00000260682.6:p.Glu122Val
ENST00000461906.1:n.390A>T
ENST00000473496.1:n.136A>T
NM_000771.3:c.365A>T	NP_000762.2:p.Glu122Val
NM_000771.4:c.365A>T MANE Select	NP_000762.2:p.Glu122Val