Canonical Allele Identifier: CA470843737

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95067319-G-T
• MyVariant Identifiers: chr10:g.96827076G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067319G>T , CM000672.2:g.95067319G>T	GRCh38
NC_000010.10:g.96827076G>T , CM000672.1:g.96827076G>T	GRCh37
NC_000010.9:g.96817066G>T	NCBI36
NG_007972.1:g.7179C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.370C>A MANE Select	ENSP00000360317.3:p.Arg124=
ENST00000371270.5:c.370C>A	ENSP00000360317.3:p.Arg124=
ENST00000479946.2:n.674C>A
ENST00000490994.6:c.*156C>A	ENSP00000433314.1:n.*156C>A
ENST00000525991.5:c.245C>A	ENSP00000433842.1:p.Pro82Gln
ENST00000526814.5:n.625C>A
ENST00000527420.5:c.370C>A	ENSP00000433191.1:p.Arg124=
ENST00000527953.5:n.625C>A
ENST00000533320.5:n.604C>A
ENST00000535898.5:c.64C>A	ENSP00000445062.1:p.Arg22=
ENST00000539050.5:c.160C>A	ENSP00000442343.2:p.Arg54=
ENST00000623108.3:c.160C>A	ENSP00000485110.1:p.Arg54=
ENST00000628935.1:c.112C>A	ENSP00000487145.1:p.Arg38=
NM_000770.3:c.370C>A MANE Select	NP_000761.3:p.Arg124=
NM_001198853.1:c.160C>A	NP_001185782.1:p.Arg54=
NM_001198854.1:c.64C>A	NP_001185783.1:p.Arg22=
NM_001198855.1:c.160C>A	NP_001185784.1:p.Arg54=
XR_945610.1:n.466C>A