Canonical Allele Identifier: CA470843688

Gene: CYP2C8

Linked Data

• dbSNP Id: rs2134442019
• MyVariant Identifiers: chr10:g.96826996G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067239G>A , CM000672.2:g.95067239G>A	GRCh38
NC_000010.10:g.96826996G>A , CM000672.1:g.96826996G>A	GRCh37
NC_000010.9:g.96816986G>A	NCBI36
NG_007972.1:g.7259C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.450C>T MANE Select	ENSP00000360317.3:p.His150=
ENST00000371270.5:c.450C>T	ENSP00000360317.3:p.His150=
ENST00000479946.2:n.754C>T
ENST00000490994.6:c.*236C>T	ENSP00000433314.1:n.*236C>T
ENST00000525991.5:c.*25C>T	ENSP00000433842.1:n.*25C>T
ENST00000526814.5:n.705C>T
ENST00000527420.5:c.450C>T	ENSP00000433191.1:p.His150=
ENST00000527953.5:n.705C>T
ENST00000533320.5:n.684C>T
ENST00000535898.5:c.144C>T	ENSP00000445062.1:p.His48=
ENST00000539050.5:c.240C>T	ENSP00000442343.2:p.His80=
ENST00000623108.3:c.240C>T	ENSP00000485110.1:p.His80=
ENST00000628935.1:c.192C>T	ENSP00000487145.1:p.His64=
NM_000770.3:c.450C>T MANE Select	NP_000761.3:p.His150=
NM_001198853.1:c.240C>T	NP_001185782.1:p.His80=
NM_001198854.1:c.144C>T	NP_001185783.1:p.His48=
NM_001198855.1:c.240C>T	NP_001185784.1:p.His80=
XR_945610.1:n.546C>T