Canonical Allele Identifier: CA211730674

Gene: CYP2C8

Linked Data

• dbSNP Id: rs923633609
• gnomAD v2: 10-96827056-G-A
• gnomAD v4: 10-95067299-G-A
• MyVariant Identifiers: chr10:g.96827056G>A (hg19) ; chr10:g.95067299G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067299G>A , CM000672.2:g.95067299G>A	GRCh38
NC_000010.10:g.96827056G>A , CM000672.1:g.96827056G>A	GRCh37
NC_000010.9:g.96817046G>A	NCBI36
NG_007972.1:g.7199C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.390C>T MANE Select	ENSP00000360317.3:p.Thr130=
ENST00000371270.5:c.390C>T	ENSP00000360317.3:p.Thr130=
ENST00000479946.2:n.694C>T
ENST00000490994.6:c.*176C>T	ENSP00000433314.1:n.*176C>T
ENST00000525991.5:c.265C>T	ENSP00000433842.1:p.Leu89Phe
ENST00000526814.5:n.645C>T
ENST00000527420.5:c.390C>T	ENSP00000433191.1:p.Thr130=
ENST00000527953.5:n.645C>T
ENST00000533320.5:n.624C>T
ENST00000535898.5:c.84C>T	ENSP00000445062.1:p.Thr28=
ENST00000539050.5:c.180C>T	ENSP00000442343.2:p.Thr60=
ENST00000623108.3:c.180C>T	ENSP00000485110.1:p.Thr60=
ENST00000628935.1:c.132C>T	ENSP00000487145.1:p.Thr44=
NM_000770.3:c.390C>T MANE Select	NP_000761.3:p.Thr130=
NM_001198853.1:c.180C>T	NP_001185782.1:p.Thr60=
NM_001198854.1:c.84C>T	NP_001185783.1:p.Thr28=
NM_001198855.1:c.180C>T	NP_001185784.1:p.Thr60=
XR_945610.1:n.486C>T