Canonical Allele Identifier: CA211711165

Gene: CYP2C8

Linked Data

• dbSNP Id: rs945544007
• gnomAD v4: 10-95036995-T-G
• MyVariant Identifiers: chr10:g.96796752T>G (hg19) ; chr10:g.95036995T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95036995T>G , CM000672.2:g.95036995T>G	GRCh38
NC_000010.10:g.96796752T>G , CM000672.1:g.96796752T>G	GRCh37
NC_000010.9:g.96786742T>G	NCBI36
NG_007972.1:g.37503A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*133A>C MANE Select	ENSP00000360317.3:n.*133A>C
ENST00000371270.5:c.*133A>C	ENSP00000360317.3:n.*133A>C
ENST00000490994.6:c.*1392A>C	ENSP00000433314.1:n.*1392A>C
ENST00000525991.5:c.*1181A>C	ENSP00000433842.1:n.*1181A>C
ENST00000526814.5:n.1861A>C
ENST00000527420.5:c.*463A>C	ENSP00000433191.1:n.*463A>C
ENST00000527953.5:n.1900A>C
ENST00000533320.5:n.1840A>C
ENST00000535898.5:c.*133A>C	ENSP00000445062.1:n.*133A>C
ENST00000539050.5:c.*133A>C	ENSP00000442343.2:n.*133A>C
ENST00000623108.3:c.*133A>C	ENSP00000485110.1:n.*133A>C
NM_000770.3:c.*133A>C MANE Select	NP_000761.3:n.*133A>C
NM_001198853.1:c.*133A>C	NP_001185782.1:n.*133A>C
NM_001198854.1:c.*133A>C	NP_001185783.1:n.*133A>C
NM_001198855.1:c.*133A>C	NP_001185784.1:n.*133A>C