Canonical Allele Identifier: CA2338188899
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949198C= , CM000681.2:g.44949198C= GRCh38
NC_000019.9:g.45452455C= , CM000681.1:g.45452455C= GRCh37
NC_000019.8:g.50144295C= NCBI36
NG_008837.1:g.8213C=

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.255C= (APOC2) MANE Select ENSP00000252490.5:p.Tyr85=
ENST00000252490.5:c.255C= (APOC4-APOC2) ENSP00000252490.4:p.Tyr85=
ENST00000585685.5:c.*1038C= (APOC4-APOC2) ENSP00000467185.1:n.*1038C=
ENST00000585786.1:c.*334C= (APOC2) ENSP00000465001.1:n.*334C=
ENST00000589057.5:c.486C= (APOC4-APOC2) ENSP00000468139.1:p.Tyr162=
ENST00000590360.2:c.255C= (APOC2) ENSP00000466775.1:p.Tyr85=
ENST00000591597.5:c.213C= (APOC2) ENSP00000476835.1:p.Tyr71=
ENST00000592257.5:c.*49C= (APOC2) ENSP00000477261.1:n.*49C=
NM_000483.4:c.255C= (APOC2) NP_000474.2:p.Tyr85=
NR_037932.1:n.1462C= (APOC4-APOC2)
NM_000483.5:c.255C= (APOC2) MANE Select NP_000474.2:p.Tyr85=