Canonical Allele Identifier: CA115620
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2580
dbSNP Id: rs120074111

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948822C>G , CM000681.2:g.44948822C>G GRCh38
NC_000019.9:g.45452079C>G , CM000681.1:g.45452079C>G GRCh37
NC_000019.8:g.50143919C>G NCBI36
NG_008837.1:g.7837C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.177C>G (APOC2) MANE Select ENSP00000252490.5:p.Tyr59Ter
ENST00000252490.5:c.177C>G (APOC4-APOC2) ENSP00000252490.4:p.Tyr59Ter
ENST00000585685.5:c.*960C>G (APOC4-APOC2) ENSP00000467185.1:n.*960C>G
ENST00000585786.1:c.177C>G (APOC2) ENSP00000465001.1:p.Tyr59Ter
ENST00000589057.5:c.408C>G (APOC4-APOC2) ENSP00000468139.1:p.Tyr136Ter
ENST00000590360.2:c.177C>G (APOC2) ENSP00000466775.1:p.Tyr59Ter
ENST00000591597.5:c.173+4C>G (APOC2) ENSP00000476835.1:n.173+4C>G
ENST00000592257.5:c.115C>G (APOC2) ENSP00000477261.1:p.Arg39Gly
NM_000483.4:c.177C>G (APOC2) NP_000474.2:p.Tyr59Ter
NR_037932.1:n.1384C>G (APOC4-APOC2)
NM_000483.5:c.177C>G (APOC2) MANE Select NP_000474.2:p.Tyr59Ter