Canonical Allele Identifier: CA406295146
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949173A>G , CM000681.2:g.44949173A>G GRCh38
NC_000019.9:g.45452430A>G , CM000681.1:g.45452430A>G GRCh37
NC_000019.8:g.50144270A>G NCBI36
NG_008837.1:g.8188A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.230A>G (APOC2) MANE Select ENSP00000252490.5:p.Lys77Arg
ENST00000252490.5:c.230A>G (APOC4-APOC2) ENSP00000252490.4:p.Lys77Arg
ENST00000585685.5:c.*1013A>G (APOC4-APOC2) ENSP00000467185.1:n.*1013A>G
ENST00000585786.1:c.*309A>G (APOC2) ENSP00000465001.1:n.*309A>G
ENST00000589057.5:c.461A>G (APOC4-APOC2) ENSP00000468139.1:p.Lys154Arg
ENST00000590360.2:c.230A>G (APOC2) ENSP00000466775.1:p.Lys77Arg
ENST00000591597.5:c.188A>G (APOC2) ENSP00000476835.1:p.Lys63Arg
ENST00000592257.5:c.*24A>G (APOC2) ENSP00000477261.1:n.*24A>G
NM_000483.4:c.230A>G (APOC2) NP_000474.2:p.Lys77Arg
NR_037932.1:n.1437A>G (APOC4-APOC2)
NM_000483.5:c.230A>G (APOC2) MANE Select NP_000474.2:p.Lys77Arg