Canonical Allele Identifier: CA1929292098

Gene: CYP2C9

Linked Data

• dbSNP Id: rs2031387681

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94941730A>G , CM000672.2:g.94941730A>G	GRCh38
NC_000010.10:g.96701487A>G , CM000672.1:g.96701487A>G	GRCh37
NC_000010.9:g.96691477A>G	NCBI36
NG_008385.1:g.8073A>G
NG_008385.2:g.8573A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.169-128A>G MANE Select	ENSP00000260682.6:n.169-128A>G
ENST00000643112.1:c.169-128A>G	ENSP00000496202.1:n.169-128A>G
ENST00000645207.1:n.194A>G
ENST00000260682.6:c.169-128A>G	ENSP00000260682.6:n.169-128A>G
ENST00000461906.1:n.194-128A>G
NM_000771.3:c.169-128A>G	NP_000762.2:n.169-128A>G
NM_000771.4:c.169-128A>G MANE Select	NP_000762.2:n.169-128A>G