Canonical Allele Identifier: CA2338188995
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949434A= , CM000681.2:g.44949434A= GRCh38
NC_000019.9:g.45452691A= , CM000681.1:g.45452691A= GRCh37
NC_000019.8:g.50144531A= NCBI36
NG_008837.1:g.8449A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.*185A= (APOC2) MANE Select ENSP00000252490.5:n.*185A=
ENST00000252490.5:c.*185A= (APOC4-APOC2) ENSP00000252490.4:n.*185A=
ENST00000585685.5:c.*1274A= (APOC4-APOC2) ENSP00000467185.1:n.*1274A=
ENST00000590360.2:c.*185A= (APOC2) ENSP00000466775.1:n.*185A=
NM_000483.4:c.*185A= (APOC2) NP_000474.2:n.*185A=
NR_037932.1:n.1698A= (APOC4-APOC2)
NM_000483.5:c.*185A= (APOC2) MANE Select NP_000474.2:n.*185A=