Canonical Allele Identifier: CA377677594

Gene: CYP2C8

Linked Data

• dbSNP Id: rs748167187
• MyVariant Identifiers: chr10:g.96797060C>G (hg19) ; chr10:g.95037303C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037303C>G , CM000672.2:g.95037303C>G	GRCh38
NC_000010.10:g.96797060C>G , CM000672.1:g.96797060C>G	GRCh37
NC_000010.9:g.96787050C>G	NCBI36
NG_007972.1:g.37195G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1298G>C MANE Select	ENSP00000360317.3:p.Arg433Pro
ENST00000371270.5:c.1298G>C	ENSP00000360317.3:p.Arg433Pro
ENST00000490994.6:c.*1084G>C	ENSP00000433314.1:n.*1084G>C
ENST00000525991.5:c.*873G>C	ENSP00000433842.1:n.*873G>C
ENST00000526814.5:n.1553G>C
ENST00000527420.5:c.*155G>C	ENSP00000433191.1:n.*155G>C
ENST00000527953.5:n.1592G>C
ENST00000531714.1:n.486G>C
ENST00000533320.5:n.1532G>C
ENST00000535898.5:c.992G>C	ENSP00000445062.1:p.Arg331Pro
ENST00000539050.5:c.1088G>C	ENSP00000442343.2:p.Arg363Pro
ENST00000623108.3:c.1088G>C	ENSP00000485110.1:p.Arg363Pro
NM_000770.3:c.1298G>C MANE Select	NP_000761.3:p.Arg433Pro
NM_001198853.1:c.1088G>C	NP_001185782.1:p.Arg363Pro
NM_001198854.1:c.992G>C	NP_001185783.1:p.Arg331Pro
NM_001198855.1:c.1088G>C	NP_001185784.1:p.Arg363Pro
XR_945610.1:n.1433G>C