Canonical Allele Identifier: CA377682651

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96826977T>C (hg19) ; chr10:g.95067220T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067220T>C , CM000672.2:g.95067220T>C	GRCh38
NC_000010.10:g.96826977T>C , CM000672.1:g.96826977T>C	GRCh37
NC_000010.9:g.96816967T>C	NCBI36
NG_007972.1:g.7278A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.469A>G MANE Select	ENSP00000360317.3:p.Arg157Gly
ENST00000371270.5:c.469A>G	ENSP00000360317.3:p.Arg157Gly
ENST00000479946.2:n.773A>G
ENST00000490994.6:c.*255A>G	ENSP00000433314.1:n.*255A>G
ENST00000525991.5:c.*44A>G	ENSP00000433842.1:n.*44A>G
ENST00000526814.5:n.724A>G
ENST00000527420.5:c.469A>G	ENSP00000433191.1:p.Arg157Gly
ENST00000527953.5:n.724A>G
ENST00000533320.5:n.703A>G
ENST00000535898.5:c.163A>G	ENSP00000445062.1:p.Arg55Gly
ENST00000539050.5:c.259A>G	ENSP00000442343.2:p.Arg87Gly
ENST00000623108.3:c.259A>G	ENSP00000485110.1:p.Arg87Gly
ENST00000628935.1:c.211A>G	ENSP00000487145.1:p.Arg71Gly
NM_000770.3:c.469A>G MANE Select	NP_000761.3:p.Arg157Gly
NM_001198853.1:c.259A>G	NP_001185782.1:p.Arg87Gly
NM_001198854.1:c.163A>G	NP_001185783.1:p.Arg55Gly
NM_001198855.1:c.259A>G	NP_001185784.1:p.Arg87Gly
XR_945610.1:n.565A>G