Canonical Allele Identifier: CA211711161

Gene: CYP2C8

Linked Data

• dbSNP Id: rs76052384
• MyVariant Identifiers: chr10:g.96796750T>A (hg19) ; chr10:g.95036993T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95036993T>A , CM000672.2:g.95036993T>A	GRCh38
NC_000010.10:g.96796750T>A , CM000672.1:g.96796750T>A	GRCh37
NC_000010.9:g.96786740T>A	NCBI36
NG_007972.1:g.37505A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*135A>T MANE Select	ENSP00000360317.3:n.*135A>T
ENST00000371270.5:c.*135A>T	ENSP00000360317.3:n.*135A>T
ENST00000490994.6:c.*1394A>T	ENSP00000433314.1:n.*1394A>T
ENST00000525991.5:c.*1183A>T	ENSP00000433842.1:n.*1183A>T
ENST00000526814.5:n.1863A>T
ENST00000527420.5:c.*465A>T	ENSP00000433191.1:n.*465A>T
ENST00000527953.5:n.1902A>T
ENST00000533320.5:n.1842A>T
ENST00000535898.5:c.*135A>T	ENSP00000445062.1:n.*135A>T
ENST00000539050.5:c.*135A>T	ENSP00000442343.2:n.*135A>T
ENST00000623108.3:c.*135A>T	ENSP00000485110.1:n.*135A>T
NM_000770.3:c.*135A>T MANE Select	NP_000761.3:n.*135A>T
NM_001198853.1:c.*135A>T	NP_001185782.1:n.*135A>T
NM_001198854.1:c.*135A>T	NP_001185783.1:n.*135A>T
NM_001198855.1:c.*135A>T	NP_001185784.1:n.*135A>T