Canonical Allele Identifier: CA2585725138
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949373T>C , CM000681.2:g.44949373T>C GRCh38
NC_000019.9:g.45452630T>C , CM000681.1:g.45452630T>C GRCh37
NC_000019.8:g.50144470T>C NCBI36
NG_008837.1:g.8388T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252490.7:c.*124T>C (APOC2) MANE Select ENSP00000252490.5:n.*124T>C
ENST00000252490.5:c.*124T>C (APOC4-APOC2) ENSP00000252490.4:n.*124T>C
ENST00000585685.5:c.*1213T>C (APOC4-APOC2) ENSP00000467185.1:n.*1213T>C
ENST00000590360.2:c.*124T>C (APOC2) ENSP00000466775.1:n.*124T>C
ENST00000591597.5:c.*124T>C (APOC2) ENSP00000476835.1:n.*124T>C
ENST00000592257.5:c.*224T>C (APOC2) ENSP00000477261.1:n.*224T>C
NM_000483.4:c.*124T>C (APOC2) NP_000474.2:n.*124T>C
NR_037932.1:n.1637T>C (APOC4-APOC2)
NM_000483.5:c.*124T>C (APOC2) MANE Select NP_000474.2:n.*124T>C