Canonical Allele Identifier: CA308876077
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1273786
ClinVar RCV Id: RCV001682249
dbSNP Id: rs4803776

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949078T>C , CM000681.2:g.44949078T>C GRCh38
NC_000019.9:g.45452335T>C , CM000681.1:g.45452335T>C GRCh37
NC_000019.8:g.50144175T>C NCBI36
NG_008837.1:g.8093T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.216-81T>C (APOC2) MANE Select ENSP00000252490.5:n.216-81T>C
ENST00000252490.5:c.216-81T>C (APOC4-APOC2) ENSP00000252490.4:n.216-81T>C
ENST00000585685.5:c.*999-81T>C (APOC4-APOC2) ENSP00000467185.1:n.*999-81T>C
ENST00000585786.1:c.*214T>C (APOC2) ENSP00000465001.1:n.*214T>C
ENST00000589057.5:c.447-81T>C (APOC4-APOC2) ENSP00000468139.1:n.447-81T>C
ENST00000590360.2:c.216-81T>C (APOC2) ENSP00000466775.1:n.216-81T>C
ENST00000591597.5:c.174-81T>C (APOC2) ENSP00000476835.1:n.174-81T>C
ENST00000592257.5:c.*10-81T>C (APOC2) ENSP00000477261.1:n.*10-81T>C
NM_000483.4:c.216-81T>C (APOC2) NP_000474.2:n.216-81T>C
NR_037932.1:n.1423-81T>C (APOC4-APOC2)
NM_000483.5:c.216-81T>C (APOC2) MANE Select NP_000474.2:n.216-81T>C