Canonical Allele Identifier: CA2610268375

Gene: CYP2C9

Linked Data

• gnomAD v4: 10-94947664-TGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94947665_94947666del , CM000672.2:g.94947665_94947666del	GRCh38
NC_000010.10:g.96707422_96707423del , CM000672.1:g.96707422_96707423del	GRCh37
NC_000010.9:g.96697412_96697413del	NCBI36
NG_008385.1:g.14008_14009del
NG_008385.2:g.14508_14509del

Transcript Alleles

HGVS	Amino-acid change
ENST00000260682.8:c.482-114_482-113del MANE Select	ENSP00000260682.6:n.482-114_482-113del
ENST00000643112.1:c.482-114_482-113del	ENSP00000496202.1:n.482-114_482-113del
ENST00000645207.1:n.635-114_635-113del
ENST00000260682.6:c.482-114_482-113del	ENSP00000260682.6:n.482-114_482-113del
ENST00000473496.1:n.253-114_253-113del
NM_000771.3:c.482-114_482-113del	NP_000762.2:n.482-114_482-113del
NM_000771.4:c.482-114_482-113del MANE Select	NP_000762.2:n.482-114_482-113del