Canonical Allele Identifier: CA5617810
Gene: CYP2C8 HGNC NCBI

Linked Data

dbSNP Id: rs369552457

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.95067344G>T , CM000672.2:g.95067344G>T GRCh38
NC_000010.10:g.96827101G>T , CM000672.1:g.96827101G>T GRCh37
NC_000010.9:g.96817091G>T NCBI36
NG_007972.1:g.7154C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371270.6:c.345C>A MANE Select ENSP00000360317.3:p.Ser115Arg
ENST00000371270.5:c.345C>A ENSP00000360317.3:p.Ser115Arg
ENST00000479946.2:n.649C>A
ENST00000490994.6:c.*131C>A ENSP00000433314.1:n.*131C>A
ENST00000525991.5:c.220C>A ENSP00000433842.1:p.Gln74Lys
ENST00000526814.5:n.600C>A
ENST00000527420.5:c.345C>A ENSP00000433191.1:p.Ser115Arg
ENST00000527953.5:n.600C>A
ENST00000533320.5:n.579C>A
ENST00000535898.5:c.39C>A ENSP00000445062.1:p.Ser13Arg
ENST00000539050.5:c.135C>A ENSP00000442343.2:p.Ser45Arg
ENST00000623108.3:c.135C>A ENSP00000485110.1:p.Ser45Arg
ENST00000628935.1:c.87C>A ENSP00000487145.1:p.Ser29Arg
NM_000770.3:c.345C>A MANE Select NP_000761.3:p.Ser115Arg
NM_001198853.1:c.135C>A NP_001185782.1:p.Ser45Arg
NM_001198854.1:c.39C>A NP_001185783.1:p.Ser13Arg
NM_001198855.1:c.135C>A NP_001185784.1:p.Ser45Arg
XR_945610.1:n.441C>A