Canonical Allele Identifier: CA2958288322

Gene: APOC2 APOC4-APOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948895C>A , CM000681.2:g.44948895C>A	GRCh38
NC_000019.9:g.45452152C>A , CM000681.1:g.45452152C>A	GRCh37
NC_000019.8:g.50143992C>A	NCBI36
NG_008837.1:g.7910C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.215+35C>A (APOC2) MANE Select	ENSP00000252490.5:n.215+35C>A
ENST00000252490.5:c.215+35C>A (APOC4-APOC2)	ENSP00000252490.4:n.215+35C>A
ENST00000585685.5:c.*998+35C>A (APOC4-APOC2)	ENSP00000467185.1:n.*998+35C>A
ENST00000585786.1:c.*31C>A (APOC2)	ENSP00000465001.1:n.*31C>A
ENST00000589057.5:c.446+35C>A (APOC4-APOC2)	ENSP00000468139.1:n.446+35C>A
ENST00000590360.2:c.215+35C>A (APOC2)	ENSP00000466775.1:n.215+35C>A
ENST00000591597.5:c.173+77C>A (APOC2)	ENSP00000476835.1:n.173+77C>A
ENST00000592257.5:c.*9+35C>A (APOC2)	ENSP00000477261.1:n.*9+35C>A
NM_000483.4:c.215+35C>A (APOC2)	NP_000474.2:n.215+35C>A
NR_037932.1:n.1422+35C>A (APOC4-APOC2)
NM_000483.5:c.215+35C>A (APOC2) MANE Select	NP_000474.2:n.215+35C>A