Canonical Allele Identifier: CA2576663948

Gene: APOC2 APOC4-APOC2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948940C>G , CM000681.2:g.44948940C>G	GRCh38
NC_000019.9:g.45452197C>G , CM000681.1:g.45452197C>G	GRCh37
NC_000019.8:g.50144037C>G	NCBI36
NG_008837.1:g.7955C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.215+80C>G (APOC2) MANE Select	ENSP00000252490.5:n.215+80C>G
ENST00000252490.5:c.215+80C>G (APOC4-APOC2)	ENSP00000252490.4:n.215+80C>G
ENST00000585685.5:c.*998+80C>G (APOC4-APOC2)	ENSP00000467185.1:n.*998+80C>G
ENST00000585786.1:c.*76C>G (APOC2)	ENSP00000465001.1:n.*76C>G
ENST00000589057.5:c.446+80C>G (APOC4-APOC2)	ENSP00000468139.1:n.446+80C>G
ENST00000590360.2:c.215+80C>G (APOC2)	ENSP00000466775.1:n.215+80C>G
ENST00000591597.5:c.173+122C>G (APOC2)	ENSP00000476835.1:n.173+122C>G
ENST00000592257.5:c.*9+80C>G (APOC2)	ENSP00000477261.1:n.*9+80C>G
NM_000483.4:c.215+80C>G (APOC2)	NP_000474.2:n.215+80C>G
NR_037932.1:n.1422+80C>G (APOC4-APOC2)
NM_000483.5:c.215+80C>G (APOC2) MANE Select	NP_000474.2:n.215+80C>G