Canonical Allele Identifier: CA15675153

Gene: CYP2C9

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94943463G>A , CM000672.2:g.94943463G>A	GRCh38
NC_000010.10:g.96703220G>A , CM000672.1:g.96703220G>A	GRCh37
NC_000010.9:g.96693210G>A	NCBI36
NG_008385.1:g.9806G>A
NG_008385.2:g.10306G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.481+1122G>A MANE Select	ENSP00000260682.6:n.481+1122G>A
ENST00000643112.1:c.481+1122G>A	ENSP00000496202.1:n.481+1122G>A
ENST00000645207.1:n.634+1122G>A
ENST00000260682.6:c.481+1122G>A	ENSP00000260682.6:n.481+1122G>A
ENST00000473496.1:n.252+1122G>A
NM_000771.3:c.481+1122G>A	NP_000762.2:n.481+1122G>A
NM_000771.4:c.481+1122G>A MANE Select	NP_000762.2:n.481+1122G>A