Canonical Allele Identifier: CA377682598

Gene: CYP2C8

Linked Data

• dbSNP Id: rs2134441922
• MyVariant Identifiers: chr10:g.96826970G>C (hg19) ; chr10:g.95067213G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067213G>C , CM000672.2:g.95067213G>C	GRCh38
NC_000010.10:g.96826970G>C , CM000672.1:g.96826970G>C	GRCh37
NC_000010.9:g.96816960G>C	NCBI36
NG_007972.1:g.7285C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.476C>G MANE Select	ENSP00000360317.3:p.Thr159Ser
ENST00000371270.5:c.476C>G	ENSP00000360317.3:p.Thr159Ser
ENST00000479946.2:n.780C>G
ENST00000490994.6:c.*262C>G	ENSP00000433314.1:n.*262C>G
ENST00000525991.5:c.*51C>G	ENSP00000433842.1:n.*51C>G
ENST00000526814.5:n.731C>G
ENST00000527420.5:c.476C>G	ENSP00000433191.1:p.Thr159Ser
ENST00000527953.5:n.731C>G
ENST00000533320.5:n.710C>G
ENST00000535898.5:c.170C>G	ENSP00000445062.1:p.Thr57Ser
ENST00000539050.5:c.266C>G	ENSP00000442343.2:p.Thr89Ser
ENST00000623108.3:c.266C>G	ENSP00000485110.1:p.Thr89Ser
ENST00000628935.1:c.218C>G	ENSP00000487145.1:p.Thr73Ser
NM_000770.3:c.476C>G MANE Select	NP_000761.3:p.Thr159Ser
NM_001198853.1:c.266C>G	NP_001185782.1:p.Thr89Ser
NM_001198854.1:c.170C>G	NP_001185783.1:p.Thr57Ser
NM_001198855.1:c.266C>G	NP_001185784.1:p.Thr89Ser
XR_945610.1:n.572C>G