Canonical Allele Identifier: CA15662925
Gene: CYP2C8 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1934953

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.95037713C>T , CM000672.2:g.95037713C>T GRCh38
NC_000010.9:g.96787460C>T NCBI36
NC_000010.10:g.96797470C>T , CM000672.1:g.96797470C>T GRCh37
NG_007972.1:g.36785G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371270.5:c.1292-404G>A ENSP00000360317.3:p.=
ENST00000490994.6:c.*1078-404G>A ENSP00000433314.1:p.=
ENST00000525991.5:c.*867-404G>A ENSP00000433842.1:p.=
ENST00000526814.5:n.1547-404G>A
ENST00000527420.5:c.*149-404G>A ENSP00000433191.1:p.=
ENST00000527953.5:n.1586-404G>A
ENST00000531714.1:n.480-404G>A
ENST00000533320.5:n.1526-404G>A
ENST00000535898.5:c.986-404G>A ENSP00000445062.1:p.=
ENST00000539050.5:c.1082-404G>A ENSP00000442343.2:p.=
ENST00000623108.3:c.1082-404G>A ENSP00000485110.1:p.=
NM_000770.3:c.1292-404G>A VV NP_000761.3:p.=
NM_001198853.1:c.1082-404G>A VV NP_001185782.1:p.=
NM_001198854.1:c.986-404G>A VV NP_001185783.1:p.=
NM_001198855.1:c.1082-404G>A VV NP_001185784.1:p.=
XR_945610.1:n.1427-404G>A