Canonical Allele Identifier: CA211730615

Gene: CYP2C8

Linked Data

• dbSNP Id: rs11572080
• MyVariant Identifiers: chr10:g.96827030C>A (hg19) ; chr10:g.95067273C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067273C>A , CM000672.2:g.95067273C>A	GRCh38
NC_000010.10:g.96827030C>A , CM000672.1:g.96827030C>A	GRCh37
NC_000010.9:g.96817020C>A	NCBI36
NG_007972.1:g.7225G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.416G>T MANE Select	ENSP00000360317.3:p.Arg139Met
ENST00000371270.5:c.416G>T	ENSP00000360317.3:p.Arg139Met
ENST00000479946.2:n.720G>T
ENST00000490994.6:c.*202G>T	ENSP00000433314.1:n.*202G>T
ENST00000525991.5:c.291G>T	ENSP00000433842.1:p.Glu97Asp
ENST00000526814.5:n.671G>T
ENST00000527420.5:c.416G>T	ENSP00000433191.1:p.Arg139Met
ENST00000527953.5:n.671G>T
ENST00000533320.5:n.650G>T
ENST00000535898.5:c.110G>T	ENSP00000445062.1:p.Arg37Met
ENST00000539050.5:c.206G>T	ENSP00000442343.2:p.Arg69Met
ENST00000623108.3:c.206G>T	ENSP00000485110.1:p.Arg69Met
ENST00000628935.1:c.158G>T	ENSP00000487145.1:p.Arg53Met
NM_000770.3:c.416G>T MANE Select	NP_000761.3:p.Arg139Met
NM_001198853.1:c.206G>T	NP_001185782.1:p.Arg69Met
NM_001198854.1:c.110G>T	NP_001185783.1:p.Arg37Met
NM_001198855.1:c.206G>T	NP_001185784.1:p.Arg69Met
XR_945610.1:n.512G>T