Canonical Allele Identifier: CA1929376067

Gene: CYP2C8

Linked Data

• dbSNP Id: rs2032914352

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037709A>T , CM000672.2:g.95037709A>T	GRCh38
NC_000010.10:g.96797466A>T , CM000672.1:g.96797466A>T	GRCh37
NC_000010.9:g.96787456A>T	NCBI36
NG_007972.1:g.36789T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1292-400T>A MANE Select	ENSP00000360317.3:n.1292-400T>A
ENST00000371270.5:c.1292-400T>A	ENSP00000360317.3:n.1292-400T>A
ENST00000490994.6:c.*1078-400T>A	ENSP00000433314.1:n.*1078-400T>A
ENST00000525991.5:c.*867-400T>A	ENSP00000433842.1:n.*867-400T>A
ENST00000526814.5:n.1547-400T>A
ENST00000527420.5:c.*149-400T>A	ENSP00000433191.1:n.*149-400T>A
ENST00000527953.5:n.1586-400T>A
ENST00000531714.1:n.480-400T>A
ENST00000533320.5:n.1526-400T>A
ENST00000535898.5:c.986-400T>A	ENSP00000445062.1:n.986-400T>A
ENST00000539050.5:c.1082-400T>A	ENSP00000442343.2:n.1082-400T>A
ENST00000623108.3:c.1082-400T>A	ENSP00000485110.1:n.1082-400T>A
NM_000770.3:c.1292-400T>A MANE Select	NP_000761.3:n.1292-400T>A
NM_001198853.1:c.1082-400T>A	NP_001185782.1:n.1082-400T>A
NM_001198854.1:c.986-400T>A	NP_001185783.1:n.986-400T>A
NM_001198855.1:c.1082-400T>A	NP_001185784.1:n.1082-400T>A
XR_945610.1:n.1427-400T>A