Canonical Allele Identifier: CA211713591

Gene: CYP2C9

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94962487G>A , CM000672.2:g.94962487G>A	GRCh38
NC_000010.10:g.96722244G>A , CM000672.1:g.96722244G>A	GRCh37
NC_000010.9:g.96712234G>A	NCBI36
NG_008385.1:g.28830G>A
NG_008385.2:g.29330G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.820-9617G>A MANE Select	ENSP00000260682.6:n.820-9617G>A
ENST00000643112.1:c.819+13203G>A	ENSP00000496202.1:n.819+13203G>A
ENST00000260682.6:c.820-9617G>A	ENSP00000260682.6:n.820-9617G>A
NM_000771.3:c.820-9617G>A	NP_000762.2:n.820-9617G>A
NM_000771.4:c.820-9617G>A MANE Select	NP_000762.2:n.820-9617G>A