Canonical Allele Identifier: CA2610269848

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95036992-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95036992G>T , CM000672.2:g.95036992G>T	GRCh38
NC_000010.10:g.96796749G>T , CM000672.1:g.96796749G>T	GRCh37
NC_000010.9:g.96786739G>T	NCBI36
NG_007972.1:g.37506C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*136C>A MANE Select	ENSP00000360317.3:n.*136C>A
ENST00000371270.5:c.*136C>A	ENSP00000360317.3:n.*136C>A
ENST00000490994.6:c.*1395C>A	ENSP00000433314.1:n.*1395C>A
ENST00000525991.5:c.*1184C>A	ENSP00000433842.1:n.*1184C>A
ENST00000526814.5:n.1864C>A
ENST00000527420.5:c.*466C>A	ENSP00000433191.1:n.*466C>A
ENST00000527953.5:n.1903C>A
ENST00000533320.5:n.1843C>A
ENST00000535898.5:c.*136C>A	ENSP00000445062.1:n.*136C>A
ENST00000539050.5:c.*136C>A	ENSP00000442343.2:n.*136C>A
ENST00000623108.3:c.*136C>A	ENSP00000485110.1:n.*136C>A
NM_000770.3:c.*136C>A MANE Select	NP_000761.3:n.*136C>A
NM_001198853.1:c.*136C>A	NP_001185782.1:n.*136C>A
NM_001198854.1:c.*136C>A	NP_001185783.1:n.*136C>A
NM_001198855.1:c.*136C>A	NP_001185784.1:n.*136C>A