Canonical Allele Identifier: CA9506567
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1374052
ClinVar RCV Id: RCV001900516
dbSNP Id: rs202190413

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948488C>T , CM000681.2:g.44948488C>T GRCh38
NC_000019.9:g.45451745C>T , CM000681.1:g.45451745C>T GRCh37
NC_000019.8:g.50143585C>T NCBI36
NG_008837.1:g.7503C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.10C>T (APOC2) MANE Select ENSP00000252490.5:p.Arg4Ter
ENST00000252490.5:c.10C>T (APOC4-APOC2) ENSP00000252490.4:p.Arg4Ter
ENST00000585685.5:c.*793C>T (APOC4-APOC2) ENSP00000467185.1:n.*793C>T
ENST00000585786.1:c.10C>T (APOC2) ENSP00000465001.1:p.Arg4Ter
ENST00000589057.5:c.241C>T (APOC4-APOC2) ENSP00000468139.1:p.Arg81Ter
ENST00000590360.2:c.10C>T (APOC2) ENSP00000466775.1:p.Arg4Ter
ENST00000591597.5:c.10C>T (APOC2) ENSP00000476835.1:p.Arg4Ter
ENST00000592257.5:c.10C>T (APOC2) ENSP00000477261.1:p.Arg4Ter
NM_000483.4:c.10C>T (APOC2) NP_000474.2:p.Arg4Ter
NR_037932.1:n.1217C>T (APOC4-APOC2)
NM_000483.5:c.10C>T (APOC2) MANE Select NP_000474.2:p.Arg4Ter