Canonical Allele Identifier: CA15662924
Gene: CYP2C8 HGNC NCBI

Linked Data

dbSNP Id: rs11572177

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.95037513T>C , CM000672.2:g.95037513T>C GRCh38
NC_000010.10:g.96797270T>C , CM000672.1:g.96797270T>C GRCh37
NC_000010.9:g.96787260T>C NCBI36
NG_007972.1:g.36985A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371270.6:c.1292-204A>G MANE Select ENSP00000360317.3:n.1292-204A>G
ENST00000371270.5:c.1292-204A>G ENSP00000360317.3:n.1292-204A>G
ENST00000490994.6:c.*1078-204A>G ENSP00000433314.1:n.*1078-204A>G
ENST00000525991.5:c.*867-204A>G ENSP00000433842.1:n.*867-204A>G
ENST00000526814.5:n.1547-204A>G
ENST00000527420.5:c.*149-204A>G ENSP00000433191.1:n.*149-204A>G
ENST00000527953.5:n.1586-204A>G
ENST00000531714.1:n.480-204A>G
ENST00000533320.5:n.1526-204A>G
ENST00000535898.5:c.986-204A>G ENSP00000445062.1:n.986-204A>G
ENST00000539050.5:c.1082-204A>G ENSP00000442343.2:n.1082-204A>G
ENST00000623108.3:c.1082-204A>G ENSP00000485110.1:n.1082-204A>G
NM_000770.3:c.1292-204A>G MANE Select NP_000761.3:n.1292-204A>G
NM_001198853.1:c.1082-204A>G NP_001185782.1:n.1082-204A>G
NM_001198854.1:c.986-204A>G NP_001185783.1:n.986-204A>G
NM_001198855.1:c.1082-204A>G NP_001185784.1:n.1082-204A>G
XR_945610.1:n.1427-204A>G