Canonical Allele Identifier: CA377683112

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1448538477
• gnomAD v2: 10-96827063-A-T
• gnomAD v4: 10-95067306-A-T
• MyVariant Identifiers: chr10:g.96827063A>T (hg19) ; chr10:g.95067306A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067306A>T , CM000672.2:g.95067306A>T	GRCh38
NC_000010.10:g.96827063A>T , CM000672.1:g.96827063A>T	GRCh37
NC_000010.9:g.96817053A>T	NCBI36
NG_007972.1:g.7192T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.383T>A MANE Select	ENSP00000360317.3:p.Leu128His
ENST00000371270.5:c.383T>A	ENSP00000360317.3:p.Leu128His
ENST00000479946.2:n.687T>A
ENST00000490994.6:c.*169T>A	ENSP00000433314.1:n.*169T>A
ENST00000525991.5:c.258T>A	ENSP00000433842.1:p.Pro86=
ENST00000526814.5:n.638T>A
ENST00000527420.5:c.383T>A	ENSP00000433191.1:p.Leu128His
ENST00000527953.5:n.638T>A
ENST00000533320.5:n.617T>A
ENST00000535898.5:c.77T>A	ENSP00000445062.1:p.Leu26His
ENST00000539050.5:c.173T>A	ENSP00000442343.2:p.Leu58His
ENST00000623108.3:c.173T>A	ENSP00000485110.1:p.Leu58His
ENST00000628935.1:c.125T>A	ENSP00000487145.1:p.Leu42His
NM_000770.3:c.383T>A MANE Select	NP_000761.3:p.Leu128His
NM_001198853.1:c.173T>A	NP_001185782.1:p.Leu58His
NM_001198854.1:c.77T>A	NP_001185783.1:p.Leu26His
NM_001198855.1:c.173T>A	NP_001185784.1:p.Leu58His
XR_945610.1:n.479T>A