Canonical Allele Identifier: CA670161334

Gene: CYP2C9

Linked Data

• dbSNP Id: rs1163443967
• MyVariant Identifiers: chr10:g.96707250T>A (hg19) ; chr10:g.94947493T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94947493T>A , CM000672.2:g.94947493T>A	GRCh38
NC_000010.10:g.96707250T>A , CM000672.1:g.96707250T>A	GRCh37
NC_000010.9:g.96697240T>A	NCBI36
NG_008385.1:g.13836T>A
NG_008385.2:g.14336T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.482-286T>A MANE Select	ENSP00000260682.6:n.482-286T>A
ENST00000643112.1:c.482-286T>A	ENSP00000496202.1:n.482-286T>A
ENST00000645207.1:n.635-286T>A
ENST00000260682.6:c.482-286T>A	ENSP00000260682.6:n.482-286T>A
ENST00000473496.1:n.253-286T>A
NM_000771.3:c.482-286T>A	NP_000762.2:n.482-286T>A
NM_000771.4:c.482-286T>A MANE Select	NP_000762.2:n.482-286T>A