Canonical Allele Identifier: CA2338188912
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949238G= , CM000681.2:g.44949238G= GRCh38
NC_000019.9:g.45452495G= , CM000681.1:g.45452495G= GRCh37
NC_000019.8:g.50144335G= NCBI36
NG_008837.1:g.8253G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.295G= (APOC2) MANE Select ENSP00000252490.5:p.Gly99=
ENST00000252490.5:c.295G= (APOC4-APOC2) ENSP00000252490.4:p.Gly99=
ENST00000585685.5:c.*1078G= (APOC4-APOC2) ENSP00000467185.1:n.*1078G=
ENST00000585786.1:c.*374G= (APOC2) ENSP00000465001.1:n.*374G=
ENST00000589057.5:c.526G= (APOC4-APOC2) ENSP00000468139.1:p.Gly176=
ENST00000590360.2:c.295G= (APOC2) ENSP00000466775.1:p.Gly99=
ENST00000591597.5:c.253G= (APOC2) ENSP00000476835.1:p.Gly85=
ENST00000592257.5:c.*89G= (APOC2) ENSP00000477261.1:n.*89G=
NM_000483.4:c.295G= (APOC2) NP_000474.2:p.Gly99=
NR_037932.1:n.1502G= (APOC4-APOC2)
NM_000483.5:c.295G= (APOC2) MANE Select NP_000474.2:p.Gly99=