Canonical Allele Identifier: CA470843706

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1589449291
• gnomAD v3: 10-95067272-C-T
• gnomAD v4: 10-95067272-C-T
• MyVariant Identifiers: chr10:g.96827029C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067272C>T , CM000672.2:g.95067272C>T	GRCh38
NC_000010.10:g.96827029C>T , CM000672.1:g.96827029C>T	GRCh37
NC_000010.9:g.96817019C>T	NCBI36
NG_007972.1:g.7226G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.417G>A MANE Select	ENSP00000360317.3:p.Arg139=
ENST00000371270.5:c.417G>A	ENSP00000360317.3:p.Arg139=
ENST00000479946.2:n.721G>A
ENST00000490994.6:c.*203G>A	ENSP00000433314.1:n.*203G>A
ENST00000525991.5:c.292G>A	ENSP00000433842.1:p.Glu98Lys
ENST00000526814.5:n.672G>A
ENST00000527420.5:c.417G>A	ENSP00000433191.1:p.Arg139=
ENST00000527953.5:n.672G>A
ENST00000533320.5:n.651G>A
ENST00000535898.5:c.111G>A	ENSP00000445062.1:p.Arg37=
ENST00000539050.5:c.207G>A	ENSP00000442343.2:p.Arg69=
ENST00000623108.3:c.207G>A	ENSP00000485110.1:p.Arg69=
ENST00000628935.1:c.159G>A	ENSP00000487145.1:p.Arg53=
NM_000770.3:c.417G>A MANE Select	NP_000761.3:p.Arg139=
NM_001198853.1:c.207G>A	NP_001185782.1:p.Arg69=
NM_001198854.1:c.111G>A	NP_001185783.1:p.Arg37=
NM_001198855.1:c.207G>A	NP_001185784.1:p.Arg69=
XR_945610.1:n.513G>A