Canonical Allele Identifier: CA470841143

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96796909G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037152G>A , CM000672.2:g.95037152G>A	GRCh38
NC_000010.10:g.96796909G>A , CM000672.1:g.96796909G>A	GRCh37
NC_000010.9:g.96786899G>A	NCBI36
NG_007972.1:g.37346C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1449C>T MANE Select	ENSP00000360317.3:p.Tyr483=
ENST00000371270.5:c.1449C>T	ENSP00000360317.3:p.Tyr483=
ENST00000490994.6:c.*1235C>T	ENSP00000433314.1:n.*1235C>T
ENST00000525991.5:c.*1024C>T	ENSP00000433842.1:n.*1024C>T
ENST00000526814.5:n.1704C>T
ENST00000527420.5:c.*306C>T	ENSP00000433191.1:n.*306C>T
ENST00000527953.5:n.1743C>T
ENST00000533320.5:n.1683C>T
ENST00000535898.5:c.1143C>T	ENSP00000445062.1:p.Tyr381=
ENST00000539050.5:c.1239C>T	ENSP00000442343.2:p.Tyr413=
ENST00000623108.3:c.1239C>T	ENSP00000485110.1:p.Tyr413=
NM_000770.3:c.1449C>T MANE Select	NP_000761.3:p.Tyr483=
NM_001198853.1:c.1239C>T	NP_001185782.1:p.Tyr413=
NM_001198854.1:c.1143C>T	NP_001185783.1:p.Tyr381=
NM_001198855.1:c.1239C>T	NP_001185784.1:p.Tyr413=