Canonical Allele Identifier: CA470841159

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96796927A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037170A>C , CM000672.2:g.95037170A>C	GRCh38
NC_000010.10:g.96796927A>C , CM000672.1:g.96796927A>C	GRCh37
NC_000010.9:g.96786917A>C	NCBI36
NG_007972.1:g.37328T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1431T>G MANE Select	ENSP00000360317.3:p.Val477=
ENST00000371270.5:c.1431T>G	ENSP00000360317.3:p.Val477=
ENST00000490994.6:c.*1217T>G	ENSP00000433314.1:n.*1217T>G
ENST00000525991.5:c.*1006T>G	ENSP00000433842.1:n.*1006T>G
ENST00000526814.5:n.1686T>G
ENST00000527420.5:c.*288T>G	ENSP00000433191.1:n.*288T>G
ENST00000527953.5:n.1725T>G
ENST00000533320.5:n.1665T>G
ENST00000535898.5:c.1125T>G	ENSP00000445062.1:p.Val375=
ENST00000539050.5:c.1221T>G	ENSP00000442343.2:p.Val407=
ENST00000623108.3:c.1221T>G	ENSP00000485110.1:p.Val407=
NM_000770.3:c.1431T>G MANE Select	NP_000761.3:p.Val477=
NM_001198853.1:c.1221T>G	NP_001185782.1:p.Val407=
NM_001198854.1:c.1125T>G	NP_001185783.1:p.Val375=
NM_001198855.1:c.1221T>G	NP_001185784.1:p.Val407=