Canonical Allele Identifier: CA2610269886

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95037045-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037045A>C , CM000672.2:g.95037045A>C	GRCh38
NC_000010.10:g.96796802A>C , CM000672.1:g.96796802A>C	GRCh37
NC_000010.9:g.96786792A>C	NCBI36
NG_007972.1:g.37453T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*83T>G MANE Select	ENSP00000360317.3:n.*83T>G
ENST00000371270.5:c.*83T>G	ENSP00000360317.3:n.*83T>G
ENST00000490994.6:c.*1342T>G	ENSP00000433314.1:n.*1342T>G
ENST00000525991.5:c.*1131T>G	ENSP00000433842.1:n.*1131T>G
ENST00000526814.5:n.1811T>G
ENST00000527420.5:c.*413T>G	ENSP00000433191.1:n.*413T>G
ENST00000527953.5:n.1850T>G
ENST00000533320.5:n.1790T>G
ENST00000535898.5:c.*83T>G	ENSP00000445062.1:n.*83T>G
ENST00000539050.5:c.*83T>G	ENSP00000442343.2:n.*83T>G
ENST00000623108.3:c.*83T>G	ENSP00000485110.1:n.*83T>G
NM_000770.3:c.*83T>G MANE Select	NP_000761.3:n.*83T>G
NM_001198853.1:c.*83T>G	NP_001185782.1:n.*83T>G
NM_001198854.1:c.*83T>G	NP_001185783.1:n.*83T>G
NM_001198855.1:c.*83T>G	NP_001185784.1:n.*83T>G