Canonical Allele Identifier: CA470843684

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96826990A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067233A>C , CM000672.2:g.95067233A>C	GRCh38
NC_000010.10:g.96826990A>C , CM000672.1:g.96826990A>C	GRCh37
NC_000010.9:g.96816980A>C	NCBI36
NG_007972.1:g.7265T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.456T>G MANE Select	ENSP00000360317.3:p.Leu152=
ENST00000371270.5:c.456T>G	ENSP00000360317.3:p.Leu152=
ENST00000479946.2:n.760T>G
ENST00000490994.6:c.*242T>G	ENSP00000433314.1:n.*242T>G
ENST00000525991.5:c.*31T>G	ENSP00000433842.1:n.*31T>G
ENST00000526814.5:n.711T>G
ENST00000527420.5:c.456T>G	ENSP00000433191.1:p.Leu152=
ENST00000527953.5:n.711T>G
ENST00000533320.5:n.690T>G
ENST00000535898.5:c.150T>G	ENSP00000445062.1:p.Leu50=
ENST00000539050.5:c.246T>G	ENSP00000442343.2:p.Leu82=
ENST00000623108.3:c.246T>G	ENSP00000485110.1:p.Leu82=
ENST00000628935.1:c.198T>G	ENSP00000487145.1:p.Leu66=
NM_000770.3:c.456T>G MANE Select	NP_000761.3:p.Leu152=
NM_001198853.1:c.246T>G	NP_001185782.1:p.Leu82=
NM_001198854.1:c.150T>G	NP_001185783.1:p.Leu50=
NM_001198855.1:c.246T>G	NP_001185784.1:p.Leu82=
XR_945610.1:n.552T>G