Canonical Allele Identifier: CA2338188721
Gene: APOC2 HGNC NCBI
APOC4-APOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44948931G= , CM000681.2:g.44948931G= GRCh38
NC_000019.9:g.45452188G= , CM000681.1:g.45452188G= GRCh37
NC_000019.8:g.50144028G= NCBI36
NG_008837.1:g.7946G=

Transcript Alleles

HGVS Amino-acid change
ENST00000252490.7:c.215+71G= (APOC2) MANE Select ENSP00000252490.5:n.215+71G=
ENST00000252490.5:c.215+71G= (APOC4-APOC2) ENSP00000252490.4:n.215+71G=
ENST00000585685.5:c.*998+71G= (APOC4-APOC2) ENSP00000467185.1:n.*998+71G=
ENST00000585786.1:c.*67G= (APOC2) ENSP00000465001.1:n.*67G=
ENST00000589057.5:c.446+71G= (APOC4-APOC2) ENSP00000468139.1:n.446+71G=
ENST00000590360.2:c.215+71G= (APOC2) ENSP00000466775.1:n.215+71G=
ENST00000591597.5:c.173+113G= (APOC2) ENSP00000476835.1:n.173+113G=
ENST00000592257.5:c.*9+71G= (APOC2) ENSP00000477261.1:n.*9+71G=
NM_000483.4:c.215+71G= (APOC2) NP_000474.2:n.215+71G=
NR_037932.1:n.1422+71G= (APOC4-APOC2)
NM_000483.5:c.215+71G= (APOC2) MANE Select NP_000474.2:n.215+71G=