Canonical Allele Identifier: CA2610269844

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95036988-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95036988T>G , CM000672.2:g.95036988T>G	GRCh38
NC_000010.10:g.96796745T>G , CM000672.1:g.96796745T>G	GRCh37
NC_000010.9:g.96786735T>G	NCBI36
NG_007972.1:g.37510A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*140A>C MANE Select	ENSP00000360317.3:n.*140A>C
ENST00000371270.5:c.*140A>C	ENSP00000360317.3:n.*140A>C
ENST00000490994.6:c.*1399A>C	ENSP00000433314.1:n.*1399A>C
ENST00000525991.5:c.*1188A>C	ENSP00000433842.1:n.*1188A>C
ENST00000526814.5:n.1868A>C
ENST00000527420.5:c.*470A>C	ENSP00000433191.1:n.*470A>C
ENST00000527953.5:n.1907A>C
ENST00000533320.5:n.1847A>C
ENST00000535898.5:c.*140A>C	ENSP00000445062.1:n.*140A>C
ENST00000539050.5:c.*140A>C	ENSP00000442343.2:n.*140A>C
ENST00000623108.3:c.*140A>C	ENSP00000485110.1:n.*140A>C
NM_000770.3:c.*140A>C MANE Select	NP_000761.3:n.*140A>C
NM_001198853.1:c.*140A>C	NP_001185782.1:n.*140A>C
NM_001198854.1:c.*140A>C	NP_001185783.1:n.*140A>C
NM_001198855.1:c.*140A>C	NP_001185784.1:n.*140A>C