Canonical Allele Identifier: CA5617808

Gene: CYP2C8

Linked Data

• dbSNP Id: rs750846477
• ExAC: 10:96827095 T / C
• gnomAD v2: 10-96827095-T-C
• gnomAD v4: 10-95067338-T-C
• MyVariant Identifiers: chr10:g.96827095T>C (hg19) ; chr10:g.95067338T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067338T>C , CM000672.2:g.95067338T>C	GRCh38
NC_000010.10:g.96827095T>C , CM000672.1:g.96827095T>C	GRCh37
NC_000010.9:g.96817085T>C	NCBI36
NG_007972.1:g.7160A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.351A>G MANE Select	ENSP00000360317.3:p.Gly117=
ENST00000371270.5:c.351A>G	ENSP00000360317.3:p.Gly117=
ENST00000479946.2:n.655A>G
ENST00000490994.6:c.*137A>G	ENSP00000433314.1:n.*137A>G
ENST00000525991.5:c.226A>G	ENSP00000433842.1:p.Lys76Glu
ENST00000526814.5:n.606A>G
ENST00000527420.5:c.351A>G	ENSP00000433191.1:p.Gly117=
ENST00000527953.5:n.606A>G
ENST00000533320.5:n.585A>G
ENST00000535898.5:c.45A>G	ENSP00000445062.1:p.Gly15=
ENST00000539050.5:c.141A>G	ENSP00000442343.2:p.Gly47=
ENST00000623108.3:c.141A>G	ENSP00000485110.1:p.Gly47=
ENST00000628935.1:c.93A>G	ENSP00000487145.1:p.Gly31=
NM_000770.3:c.351A>G MANE Select	NP_000761.3:p.Gly117=
NM_001198853.1:c.141A>G	NP_001185782.1:p.Gly47=
NM_001198854.1:c.45A>G	NP_001185783.1:p.Gly15=
NM_001198855.1:c.141A>G	NP_001185784.1:p.Gly47=
XR_945610.1:n.447A>G