Canonical Allele Identifier: CA470841149

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96796918T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037161T>A , CM000672.2:g.95037161T>A	GRCh38
NC_000010.10:g.96796918T>A , CM000672.1:g.96796918T>A	GRCh37
NC_000010.9:g.96786908T>A	NCBI36
NG_007972.1:g.37337A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1440A>T MANE Select	ENSP00000360317.3:p.Pro480=
ENST00000371270.5:c.1440A>T	ENSP00000360317.3:p.Pro480=
ENST00000490994.6:c.*1226A>T	ENSP00000433314.1:n.*1226A>T
ENST00000525991.5:c.*1015A>T	ENSP00000433842.1:n.*1015A>T
ENST00000526814.5:n.1695A>T
ENST00000527420.5:c.*297A>T	ENSP00000433191.1:n.*297A>T
ENST00000527953.5:n.1734A>T
ENST00000533320.5:n.1674A>T
ENST00000535898.5:c.1134A>T	ENSP00000445062.1:p.Pro378=
ENST00000539050.5:c.1230A>T	ENSP00000442343.2:p.Pro410=
ENST00000623108.3:c.1230A>T	ENSP00000485110.1:p.Pro410=
NM_000770.3:c.1440A>T MANE Select	NP_000761.3:p.Pro480=
NM_001198853.1:c.1230A>T	NP_001185782.1:p.Pro410=
NM_001198854.1:c.1134A>T	NP_001185783.1:p.Pro378=
NM_001198855.1:c.1230A>T	NP_001185784.1:p.Pro410=