Canonical Allele Identifier: CA2585725085

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v4: 19-44949318-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949318A>G , CM000681.2:g.44949318A>G	GRCh38
NC_000019.9:g.45452575A>G , CM000681.1:g.45452575A>G	GRCh37
NC_000019.8:g.50144415A>G	NCBI36
NG_008837.1:g.8333A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.*69A>G (APOC2) MANE Select	ENSP00000252490.5:n.*69A>G
ENST00000252490.5:c.*69A>G (APOC4-APOC2)	ENSP00000252490.4:n.*69A>G
ENST00000585685.5:c.*1158A>G (APOC4-APOC2)	ENSP00000467185.1:n.*1158A>G
ENST00000585786.1:c.*454A>G (APOC2)	ENSP00000465001.1:n.*454A>G
ENST00000589057.5:c.*69A>G (APOC4-APOC2)	ENSP00000468139.1:n.*69A>G
ENST00000590360.2:c.*69A>G (APOC2)	ENSP00000466775.1:n.*69A>G
ENST00000591597.5:c.*69A>G (APOC2)	ENSP00000476835.1:n.*69A>G
ENST00000592257.5:c.*169A>G (APOC2)	ENSP00000477261.1:n.*169A>G
NM_000483.4:c.*69A>G (APOC2)	NP_000474.2:n.*69A>G
NR_037932.1:n.1582A>G (APOC4-APOC2)
NM_000483.5:c.*69A>G (APOC2) MANE Select	NP_000474.2:n.*69A>G