Canonical Allele Identifier: CA2338188686
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948846A= , CM000681.2:g.44948846A= GRCh38
NC_000019.9:g.45452103A= , CM000681.1:g.45452103A= GRCh37
NC_000019.8:g.50143943A= NCBI36
NG_008837.1:g.7861A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.201A= (APOC2) MANE Select ENSP00000252490.5:p.Val67=
ENST00000252490.5:c.201A= (APOC4-APOC2) ENSP00000252490.4:p.Val67=
ENST00000585685.5:c.*984A= (APOC4-APOC2) ENSP00000467185.1:n.*984A=
ENST00000585786.1:c.201A= (APOC2) ENSP00000465001.1:p.Val67=
ENST00000589057.5:c.432A= (APOC4-APOC2) ENSP00000468139.1:p.Val144=
ENST00000590360.2:c.201A= (APOC2) ENSP00000466775.1:p.Val67=
ENST00000591597.5:c.173+28A= (APOC2) ENSP00000476835.1:n.173+28A=
ENST00000592257.5:c.139A= (APOC2) ENSP00000477261.1:p.Arg47=
NM_000483.4:c.201A= (APOC2) NP_000474.2:p.Val67=
NR_037932.1:n.1408A= (APOC4-APOC2)
NM_000483.5:c.201A= (APOC2) MANE Select NP_000474.2:p.Val67=