Canonical Allele Identifier: CA406295225
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949187A>C , CM000681.2:g.44949187A>C GRCh38
NC_000019.9:g.45452444A>C , CM000681.1:g.45452444A>C GRCh37
NC_000019.8:g.50144284A>C NCBI36
NG_008837.1:g.8202A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.244A>C (APOC2) MANE Select ENSP00000252490.5:p.Met82Leu
ENST00000252490.5:c.244A>C (APOC4-APOC2) ENSP00000252490.4:p.Met82Leu
ENST00000585685.5:c.*1027A>C (APOC4-APOC2) ENSP00000467185.1:n.*1027A>C
ENST00000585786.1:c.*323A>C (APOC2) ENSP00000465001.1:n.*323A>C
ENST00000589057.5:c.475A>C (APOC4-APOC2) ENSP00000468139.1:p.Met159Leu
ENST00000590360.2:c.244A>C (APOC2) ENSP00000466775.1:p.Met82Leu
ENST00000591597.5:c.202A>C (APOC2) ENSP00000476835.1:p.Met68Leu
ENST00000592257.5:c.*38A>C (APOC2) ENSP00000477261.1:n.*38A>C
NM_000483.4:c.244A>C (APOC2) NP_000474.2:p.Met82Leu
NR_037932.1:n.1451A>C (APOC4-APOC2)
NM_000483.5:c.244A>C (APOC2) MANE Select NP_000474.2:p.Met82Leu