Canonical Allele Identifier: CA406295238
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

dbSNP Id: rs1230631209

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949188T>C , CM000681.2:g.44949188T>C GRCh38
NC_000019.9:g.45452445T>C , CM000681.1:g.45452445T>C GRCh37
NC_000019.8:g.50144285T>C NCBI36
NG_008837.1:g.8203T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.245T>C (APOC2) MANE Select ENSP00000252490.5:p.Met82Thr
ENST00000252490.5:c.245T>C (APOC4-APOC2) ENSP00000252490.4:p.Met82Thr
ENST00000585685.5:c.*1028T>C (APOC4-APOC2) ENSP00000467185.1:n.*1028T>C
ENST00000585786.1:c.*324T>C (APOC2) ENSP00000465001.1:n.*324T>C
ENST00000589057.5:c.476T>C (APOC4-APOC2) ENSP00000468139.1:p.Met159Thr
ENST00000590360.2:c.245T>C (APOC2) ENSP00000466775.1:p.Met82Thr
ENST00000591597.5:c.203T>C (APOC2) ENSP00000476835.1:p.Met68Thr
ENST00000592257.5:c.*39T>C (APOC2) ENSP00000477261.1:n.*39T>C
NM_000483.4:c.245T>C (APOC2) NP_000474.2:p.Met82Thr
NR_037932.1:n.1452T>C (APOC4-APOC2)
NM_000483.5:c.245T>C (APOC2) MANE Select NP_000474.2:p.Met82Thr