Canonical Allele Identifier: CA377676974

Gene: CYP2C9

Linked Data

• MyVariant Identifiers: chr10:g.96748669T>A (hg19) ; chr10:g.94988912T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94988912T>A , CM000672.2:g.94988912T>A	GRCh38
NC_000010.10:g.96748669T>A , CM000672.1:g.96748669T>A	GRCh37
NC_000010.9:g.96738659T>A	NCBI36
NG_008385.1:g.55255T>A
NG_008385.2:g.55755T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.1357T>A MANE Select	ENSP00000260682.6:p.Leu453Ile
ENST00000643112.1:c.*366T>A	ENSP00000496202.1:n.*366T>A
ENST00000260682.6:c.1357T>A	ENSP00000260682.6:p.Leu453Ile
NM_000771.3:c.1357T>A	NP_000762.2:p.Leu453Ile
NM_000771.4:c.1357T>A MANE Select	NP_000762.2:p.Leu453Ile