Canonical Allele Identifier: CA470837364

Gene: CYP2C9

Linked Data

• gnomAD v4: 10-94988873-C-T
• MyVariant Identifiers: chr10:g.96748630C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94988873C>T , CM000672.2:g.94988873C>T	GRCh38
NC_000010.10:g.96748630C>T , CM000672.1:g.96748630C>T	GRCh37
NC_000010.9:g.96738620C>T	NCBI36
NG_008385.1:g.55216C>T
NG_008385.2:g.55716C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.1318C>T MANE Select	ENSP00000260682.6:p.Leu440=
ENST00000643112.1:c.*327C>T	ENSP00000496202.1:n.*327C>T
ENST00000260682.6:c.1318C>T	ENSP00000260682.6:p.Leu440=
NM_000771.3:c.1318C>T	NP_000762.2:p.Leu440=
NM_000771.4:c.1318C>T MANE Select	NP_000762.2:p.Leu440=