Canonical Allele Identifier: CA2610268010

Gene: CYP2C9

Linked Data

• gnomAD v4: 10-94942590-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942596del , CM000672.2:g.94942596del	GRCh38
NC_000010.10:g.96702353del , CM000672.1:g.96702353del	GRCh37
NC_000010.9:g.96692343del	NCBI36
NG_008385.1:g.8939del
NG_008385.2:g.9439del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.481+255del MANE Select	ENSP00000260682.6:n.481+255del
ENST00000643112.1:c.481+255del	ENSP00000496202.1:n.481+255del
ENST00000645207.1:n.634+255del
ENST00000260682.6:c.481+255del	ENSP00000260682.6:n.481+255del
ENST00000461906.1:n.761del
ENST00000473496.1:n.252+255del
NM_000771.3:c.481+255del	NP_000762.2:n.481+255del
NM_000771.4:c.481+255del MANE Select	NP_000762.2:n.481+255del