Canonical Allele Identifier: CA2580598889

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94981669C>A , CM000672.2:g.94981669C>A	GRCh38
NC_000010.10:g.96741426C>A , CM000672.1:g.96741426C>A	GRCh37
NC_000010.9:g.96731416C>A	NCBI36
NG_008385.1:g.48012C>A
NG_008385.2:g.48512C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.1149+299C>A MANE Select	ENSP00000260682.6:n.1149+299C>A
ENST00000643112.1:c.*158+299C>A	ENSP00000496202.1:n.*158+299C>A
ENST00000260682.6:c.1149+299C>A	ENSP00000260682.6:n.1149+299C>A
NM_000771.3:c.1149+299C>A	NP_000762.2:n.1149+299C>A
NM_000771.4:c.1149+299C>A MANE Select	NP_000762.2:n.1149+299C>A