Canonical Allele Identifier: CA470843679

Gene: CYP2C8

Linked Data

• dbSNP Id: rs2134441971
• MyVariant Identifiers: chr10:g.96826981C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067224C>T , CM000672.2:g.95067224C>T	GRCh38
NC_000010.10:g.96826981C>T , CM000672.1:g.96826981C>T	GRCh37
NC_000010.9:g.96816971C>T	NCBI36
NG_007972.1:g.7274G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.465G>A MANE Select	ENSP00000360317.3:p.Glu155=
ENST00000371270.5:c.465G>A	ENSP00000360317.3:p.Glu155=
ENST00000479946.2:n.769G>A
ENST00000490994.6:c.*251G>A	ENSP00000433314.1:n.*251G>A
ENST00000525991.5:c.*40G>A	ENSP00000433842.1:n.*40G>A
ENST00000526814.5:n.720G>A
ENST00000527420.5:c.465G>A	ENSP00000433191.1:p.Glu155=
ENST00000527953.5:n.720G>A
ENST00000533320.5:n.699G>A
ENST00000535898.5:c.159G>A	ENSP00000445062.1:p.Glu53=
ENST00000539050.5:c.255G>A	ENSP00000442343.2:p.Glu85=
ENST00000623108.3:c.255G>A	ENSP00000485110.1:p.Glu85=
ENST00000628935.1:c.207G>A	ENSP00000487145.1:p.Glu69=
NM_000770.3:c.465G>A MANE Select	NP_000761.3:p.Glu155=
NM_001198853.1:c.255G>A	NP_001185782.1:p.Glu85=
NM_001198854.1:c.159G>A	NP_001185783.1:p.Glu53=
NM_001198855.1:c.255G>A	NP_001185784.1:p.Glu85=
XR_945610.1:n.561G>A