Canonical Allele Identifier: CA2585725236
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949456A>C , CM000681.2:g.44949456A>C GRCh38
NC_000019.9:g.45452713A>C , CM000681.1:g.45452713A>C GRCh37
NC_000019.8:g.50144553A>C NCBI36
NG_008837.1:g.8471A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.*207A>C (APOC2) MANE Select ENSP00000252490.5:n.*207A>C
ENST00000252490.5:c.*207A>C (APOC4-APOC2) ENSP00000252490.4:n.*207A>C
ENST00000585685.5:c.*1296A>C (APOC4-APOC2) ENSP00000467185.1:n.*1296A>C
ENST00000590360.2:c.*207A>C (APOC2) ENSP00000466775.1:n.*207A>C
NM_000483.4:c.*207A>C (APOC2) NP_000474.2:n.*207A>C
NR_037932.1:n.1720A>C (APOC4-APOC2)
NM_000483.5:c.*207A>C (APOC2) MANE Select NP_000474.2:n.*207A>C