Canonical Allele Identifier: CA2338188626
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948479A= , CM000681.2:g.44948479A= GRCh38
NC_000019.9:g.45451736A= , CM000681.1:g.45451736A= GRCh37
NC_000019.8:g.50143576A= NCBI36
NG_008837.1:g.7494A=

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.1A= (APOC2) MANE Select ENSP00000252490.5:p.Met1=
ENST00000252490.5:c.1A= (APOC4-APOC2) ENSP00000252490.4:p.Met1=
ENST00000585685.5:c.*784A= (APOC4-APOC2) ENSP00000467185.1:n.*784A=
ENST00000585786.1:c.1A= (APOC2) ENSP00000465001.1:p.Met1=
ENST00000589057.5:c.232A= (APOC4-APOC2) ENSP00000468139.1:p.Met78=
ENST00000590360.2:c.1A= (APOC2) ENSP00000466775.1:p.Met1=
ENST00000591597.5:c.1A= (APOC2) ENSP00000476835.1:p.Met1=
ENST00000592257.5:c.1A= (APOC2) ENSP00000477261.1:p.Met1=
NM_000483.4:c.1A= (APOC2) NP_000474.2:p.Met1=
NR_037932.1:n.1208A= (APOC4-APOC2)
NM_000483.5:c.1A= (APOC2) MANE Select NP_000474.2:p.Met1=