Canonical Allele Identifier: CA2585725086
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949320C>A , CM000681.2:g.44949320C>A GRCh38
NC_000019.9:g.45452577C>A , CM000681.1:g.45452577C>A GRCh37
NC_000019.8:g.50144417C>A NCBI36
NG_008837.1:g.8335C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.*71C>A (APOC2) MANE Select ENSP00000252490.5:n.*71C>A
ENST00000252490.5:c.*71C>A (APOC4-APOC2) ENSP00000252490.4:n.*71C>A
ENST00000585685.5:c.*1160C>A (APOC4-APOC2) ENSP00000467185.1:n.*1160C>A
ENST00000585786.1:c.*456C>A (APOC2) ENSP00000465001.1:n.*456C>A
ENST00000589057.5:c.*71C>A (APOC4-APOC2) ENSP00000468139.1:n.*71C>A
ENST00000590360.2:c.*71C>A (APOC2) ENSP00000466775.1:n.*71C>A
ENST00000591597.5:c.*71C>A (APOC2) ENSP00000476835.1:n.*71C>A
ENST00000592257.5:c.*171C>A (APOC2) ENSP00000477261.1:n.*171C>A
NM_000483.4:c.*71C>A (APOC2) NP_000474.2:n.*71C>A
NR_037932.1:n.1584C>A (APOC4-APOC2)
NM_000483.5:c.*71C>A (APOC2) MANE Select NP_000474.2:n.*71C>A