Canonical Allele Identifier: CA470843694

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96827008T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067251T>C , CM000672.2:g.95067251T>C	GRCh38
NC_000010.10:g.96827008T>C , CM000672.1:g.96827008T>C	GRCh37
NC_000010.9:g.96816998T>C	NCBI36
NG_007972.1:g.7247A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.438A>G MANE Select	ENSP00000360317.3:p.Gln146=
ENST00000371270.5:c.438A>G	ENSP00000360317.3:p.Gln146=
ENST00000479946.2:n.742A>G
ENST00000490994.6:c.*224A>G	ENSP00000433314.1:n.*224A>G
ENST00000525991.5:c.*13A>G	ENSP00000433842.1:n.*13A>G
ENST00000526814.5:n.693A>G
ENST00000527420.5:c.438A>G	ENSP00000433191.1:p.Gln146=
ENST00000527953.5:n.693A>G
ENST00000533320.5:n.672A>G
ENST00000535898.5:c.132A>G	ENSP00000445062.1:p.Gln44=
ENST00000539050.5:c.228A>G	ENSP00000442343.2:p.Gln76=
ENST00000623108.3:c.228A>G	ENSP00000485110.1:p.Gln76=
ENST00000628935.1:c.180A>G	ENSP00000487145.1:p.Gln60=
NM_000770.3:c.438A>G MANE Select	NP_000761.3:p.Gln146=
NM_001198853.1:c.228A>G	NP_001185782.1:p.Gln76=
NM_001198854.1:c.132A>G	NP_001185783.1:p.Gln44=
NM_001198855.1:c.228A>G	NP_001185784.1:p.Gln76=
XR_945610.1:n.534A>G