Canonical Allele Identifier: CA377677337

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95037183-G-A
• MyVariant Identifiers: chr10:g.96796940G>A (hg19) ; chr10:g.95037183G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037183G>A , CM000672.2:g.95037183G>A	GRCh38
NC_000010.10:g.96796940G>A , CM000672.1:g.96796940G>A	GRCh37
NC_000010.9:g.96786930G>A	NCBI36
NG_007972.1:g.37315C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1418C>T MANE Select	ENSP00000360317.3:p.Thr473Ile
ENST00000371270.5:c.1418C>T	ENSP00000360317.3:p.Thr473Ile
ENST00000490994.6:c.*1204C>T	ENSP00000433314.1:n.*1204C>T
ENST00000525991.5:c.*993C>T	ENSP00000433842.1:n.*993C>T
ENST00000526814.5:n.1673C>T
ENST00000527420.5:c.*275C>T	ENSP00000433191.1:n.*275C>T
ENST00000527953.5:n.1712C>T
ENST00000531714.1:n.606C>T
ENST00000533320.5:n.1652C>T
ENST00000535898.5:c.1112C>T	ENSP00000445062.1:p.Thr371Ile
ENST00000539050.5:c.1208C>T	ENSP00000442343.2:p.Thr403Ile
ENST00000623108.3:c.1208C>T	ENSP00000485110.1:p.Thr403Ile
NM_000770.3:c.1418C>T MANE Select	NP_000761.3:p.Thr473Ile
NM_001198853.1:c.1208C>T	NP_001185782.1:p.Thr403Ile
NM_001198854.1:c.1112C>T	NP_001185783.1:p.Thr371Ile
NM_001198855.1:c.1208C>T	NP_001185784.1:p.Thr403Ile
XR_945610.1:n.1553C>T