Canonical Allele Identifier: CA470843689

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96826999A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067242A>C , CM000672.2:g.95067242A>C	GRCh38
NC_000010.10:g.96826999A>C , CM000672.1:g.96826999A>C	GRCh37
NC_000010.9:g.96816989A>C	NCBI36
NG_007972.1:g.7256T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.447T>G MANE Select	ENSP00000360317.3:p.Ala149=
ENST00000371270.5:c.447T>G	ENSP00000360317.3:p.Ala149=
ENST00000479946.2:n.751T>G
ENST00000490994.6:c.*233T>G	ENSP00000433314.1:n.*233T>G
ENST00000525991.5:c.*22T>G	ENSP00000433842.1:n.*22T>G
ENST00000526814.5:n.702T>G
ENST00000527420.5:c.447T>G	ENSP00000433191.1:p.Ala149=
ENST00000527953.5:n.702T>G
ENST00000533320.5:n.681T>G
ENST00000535898.5:c.141T>G	ENSP00000445062.1:p.Ala47=
ENST00000539050.5:c.237T>G	ENSP00000442343.2:p.Ala79=
ENST00000623108.3:c.237T>G	ENSP00000485110.1:p.Ala79=
ENST00000628935.1:c.189T>G	ENSP00000487145.1:p.Ala63=
NM_000770.3:c.447T>G MANE Select	NP_000761.3:p.Ala149=
NM_001198853.1:c.237T>G	NP_001185782.1:p.Ala79=
NM_001198854.1:c.141T>G	NP_001185783.1:p.Ala47=
NM_001198855.1:c.237T>G	NP_001185784.1:p.Ala79=
XR_945610.1:n.543T>G