Canonical Allele Identifier: CA10576168

Gene: CYP2C9

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94965778A>C , CM000672.2:g.94965778A>C	GRCh38
NC_000010.10:g.96725535A>C , CM000672.1:g.96725535A>C	GRCh37
NC_000010.9:g.96715525A>C	NCBI36
NG_008385.1:g.32121A>C
NG_008385.2:g.32621A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.820-6326A>C MANE Select	ENSP00000260682.6:n.820-6326A>C
ENST00000643112.1:c.820-15405A>C	ENSP00000496202.1:n.820-15405A>C
ENST00000260682.6:c.820-6326A>C	ENSP00000260682.6:n.820-6326A>C
NM_000771.3:c.820-6326A>C	NP_000762.2:n.820-6326A>C
NM_000771.4:c.820-6326A>C MANE Select	NP_000762.2:n.820-6326A>C