Canonical Allele Identifier: CA2735916380
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Linked Data

dbSNP Id: rs1970360110

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44949386T>A , CM000681.2:g.44949386T>A GRCh38
NC_000019.9:g.45452643T>A , CM000681.1:g.45452643T>A GRCh37
NC_000019.8:g.50144483T>A NCBI36
NG_008837.1:g.8401T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.*137T>A (APOC2) MANE Select ENSP00000252490.5:n.*137T>A
ENST00000252490.5:c.*137T>A (APOC4-APOC2) ENSP00000252490.4:n.*137T>A
ENST00000585685.5:c.*1226T>A (APOC4-APOC2) ENSP00000467185.1:n.*1226T>A
ENST00000590360.2:c.*137T>A (APOC2) ENSP00000466775.1:n.*137T>A
ENST00000591597.5:c.*137T>A (APOC2) ENSP00000476835.1:n.*137T>A
ENST00000592257.5:c.*237T>A (APOC2) ENSP00000477261.1:n.*237T>A
NM_000483.4:c.*137T>A (APOC2) NP_000474.2:n.*137T>A
NR_037932.1:n.1650T>A (APOC4-APOC2)
NM_000483.5:c.*137T>A (APOC2) MANE Select NP_000474.2:n.*137T>A