Canonical Allele Identifier: CA2574620329

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95037055-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037055A>G , CM000672.2:g.95037055A>G	GRCh38
NC_000010.10:g.96796812A>G , CM000672.1:g.96796812A>G	GRCh37
NC_000010.9:g.96786802A>G	NCBI36
NG_007972.1:g.37443T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*73T>C MANE Select	ENSP00000360317.3:n.*73T>C
ENST00000371270.5:c.*73T>C	ENSP00000360317.3:n.*73T>C
ENST00000490994.6:c.*1332T>C	ENSP00000433314.1:n.*1332T>C
ENST00000525991.5:c.*1121T>C	ENSP00000433842.1:n.*1121T>C
ENST00000526814.5:n.1801T>C
ENST00000527420.5:c.*403T>C	ENSP00000433191.1:n.*403T>C
ENST00000527953.5:n.1840T>C
ENST00000533320.5:n.1780T>C
ENST00000535898.5:c.*73T>C	ENSP00000445062.1:n.*73T>C
ENST00000539050.5:c.*73T>C	ENSP00000442343.2:n.*73T>C
ENST00000623108.3:c.*73T>C	ENSP00000485110.1:n.*73T>C
NM_000770.3:c.*73T>C MANE Select	NP_000761.3:n.*73T>C
NM_001198853.1:c.*73T>C	NP_001185782.1:n.*73T>C
NM_001198854.1:c.*73T>C	NP_001185783.1:n.*73T>C
NM_001198855.1:c.*73T>C	NP_001185784.1:n.*73T>C