Canonical Allele Identifier: CA996271355

Gene: APOC2 APOC4-APOC2

Linked Data

• dbSNP Id: rs1970353366
• gnomAD v3: 19-44948966-G-A
• gnomAD v4: 19-44948966-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44948966G>A , CM000681.2:g.44948966G>A	GRCh38
NC_000019.9:g.45452223G>A , CM000681.1:g.45452223G>A	GRCh37
NC_000019.8:g.50144063G>A	NCBI36
NG_008837.1:g.7981G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.215+106G>A (APOC2) MANE Select	ENSP00000252490.5:n.215+106G>A
ENST00000252490.5:c.215+106G>A (APOC4-APOC2)	ENSP00000252490.4:n.215+106G>A
ENST00000585685.5:c.*998+106G>A (APOC4-APOC2)	ENSP00000467185.1:n.*998+106G>A
ENST00000585786.1:c.*102G>A (APOC2)	ENSP00000465001.1:n.*102G>A
ENST00000589057.5:c.446+106G>A (APOC4-APOC2)	ENSP00000468139.1:n.446+106G>A
ENST00000590360.2:c.215+106G>A (APOC2)	ENSP00000466775.1:n.215+106G>A
ENST00000591597.5:c.173+148G>A (APOC2)	ENSP00000476835.1:n.173+148G>A
ENST00000592257.5:c.*9+106G>A (APOC2)	ENSP00000477261.1:n.*9+106G>A
NM_000483.4:c.215+106G>A (APOC2)	NP_000474.2:n.215+106G>A
NR_037932.1:n.1422+106G>A (APOC4-APOC2)
NM_000483.5:c.215+106G>A (APOC2) MANE Select	NP_000474.2:n.215+106G>A