Canonical Allele Identifier: CA377682826

Gene: CYP2C8

Linked Data

• dbSNP Id: rs2033588864
• MyVariant Identifiers: chr10:g.96827010G>A (hg19) ; chr10:g.95067253G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067253G>A , CM000672.2:g.95067253G>A	GRCh38
NC_000010.10:g.96827010G>A , CM000672.1:g.96827010G>A	GRCh37
NC_000010.9:g.96817000G>A	NCBI36
NG_007972.1:g.7245C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.436C>T MANE Select	ENSP00000360317.3:p.Gln146Ter
ENST00000371270.5:c.436C>T	ENSP00000360317.3:p.Gln146Ter
ENST00000479946.2:n.740C>T
ENST00000490994.6:c.*222C>T	ENSP00000433314.1:n.*222C>T
ENST00000525991.5:c.*11C>T	ENSP00000433842.1:n.*11C>T
ENST00000526814.5:n.691C>T
ENST00000527420.5:c.436C>T	ENSP00000433191.1:p.Gln146Ter
ENST00000527953.5:n.691C>T
ENST00000533320.5:n.670C>T
ENST00000535898.5:c.130C>T	ENSP00000445062.1:p.Gln44Ter
ENST00000539050.5:c.226C>T	ENSP00000442343.2:p.Gln76Ter
ENST00000623108.3:c.226C>T	ENSP00000485110.1:p.Gln76Ter
ENST00000628935.1:c.178C>T	ENSP00000487145.1:p.Gln60Ter
NM_000770.3:c.436C>T MANE Select	NP_000761.3:p.Gln146Ter
NM_001198853.1:c.226C>T	NP_001185782.1:p.Gln76Ter
NM_001198854.1:c.130C>T	NP_001185783.1:p.Gln44Ter
NM_001198855.1:c.226C>T	NP_001185784.1:p.Gln76Ter
XR_945610.1:n.532C>T