Canonical Allele Identifier: CA2610269911

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95037098-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037098C>A , CM000672.2:g.95037098C>A	GRCh38
NC_000010.10:g.96796855C>A , CM000672.1:g.96796855C>A	GRCh37
NC_000010.9:g.96786845C>A	NCBI36
NG_007972.1:g.37400G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*30G>T MANE Select	ENSP00000360317.3:n.*30G>T
ENST00000371270.5:c.*30G>T	ENSP00000360317.3:n.*30G>T
ENST00000490994.6:c.*1289G>T	ENSP00000433314.1:n.*1289G>T
ENST00000525991.5:c.*1078G>T	ENSP00000433842.1:n.*1078G>T
ENST00000526814.5:n.1758G>T
ENST00000527420.5:c.*360G>T	ENSP00000433191.1:n.*360G>T
ENST00000527953.5:n.1797G>T
ENST00000533320.5:n.1737G>T
ENST00000535898.5:c.*30G>T	ENSP00000445062.1:n.*30G>T
ENST00000539050.5:c.*30G>T	ENSP00000442343.2:n.*30G>T
ENST00000623108.3:c.*30G>T	ENSP00000485110.1:n.*30G>T
NM_000770.3:c.*30G>T MANE Select	NP_000761.3:n.*30G>T
NM_001198853.1:c.*30G>T	NP_001185782.1:n.*30G>T
NM_001198854.1:c.*30G>T	NP_001185783.1:n.*30G>T
NM_001198855.1:c.*30G>T	NP_001185784.1:n.*30G>T