Canonical Allele Identifier: CA2338188684
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948843T= , CM000681.2:g.44948843T= GRCh38
NC_000019.9:g.45452100T= , CM000681.1:g.45452100T= GRCh37
NC_000019.8:g.50143940T= NCBI36
NG_008837.1:g.7858T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.198T= (APOC2) MANE Select ENSP00000252490.5:p.Ala66=
ENST00000252490.5:c.198T= (APOC4-APOC2) ENSP00000252490.4:p.Ala66=
ENST00000585685.5:c.*981T= (APOC4-APOC2) ENSP00000467185.1:n.*981T=
ENST00000585786.1:c.198T= (APOC2) ENSP00000465001.1:p.Ala66=
ENST00000589057.5:c.429T= (APOC4-APOC2) ENSP00000468139.1:p.Ala143=
ENST00000590360.2:c.198T= (APOC2) ENSP00000466775.1:p.Ala66=
ENST00000591597.5:c.173+25T= (APOC2) ENSP00000476835.1:n.173+25T=
ENST00000592257.5:c.136T= (APOC2) ENSP00000477261.1:p.Cys46=
NM_000483.4:c.198T= (APOC2) NP_000474.2:p.Ala66=
NR_037932.1:n.1405T= (APOC4-APOC2)
NM_000483.5:c.198T= (APOC2) MANE Select NP_000474.2:p.Ala66=