Canonical Allele Identifier: CA377677047

Gene: CYP2C9

Linked Data

• COSMIC: COSM1702816
• MyVariant Identifiers: chr10:g.96748702C>T (hg19) ; chr10:g.94988945C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94988945C>T , CM000672.2:g.94988945C>T	GRCh38
NC_000010.10:g.96748702C>T , CM000672.1:g.96748702C>T	GRCh37
NC_000010.9:g.96738692C>T	NCBI36
NG_008385.1:g.55288C>T
NG_008385.2:g.55788C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260682.8:c.1390C>T MANE Select	ENSP00000260682.6:p.Pro464Ser
ENST00000643112.1:c.*399C>T	ENSP00000496202.1:n.*399C>T
ENST00000260682.6:c.1390C>T	ENSP00000260682.6:p.Pro464Ser
NM_000771.3:c.1390C>T	NP_000762.2:p.Pro464Ser
NM_000771.4:c.1390C>T MANE Select	NP_000762.2:p.Pro464Ser