Canonical Allele Identifier: CA507796214

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v4: 19-44949201-A-G
• MyVariant Identifiers: chr19:g.45452458A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949201A>G , CM000681.2:g.44949201A>G	GRCh38
NC_000019.9:g.45452458A>G , CM000681.1:g.45452458A>G	GRCh37
NC_000019.8:g.50144298A>G	NCBI36
NG_008837.1:g.8216A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.258A>G (APOC2) MANE Select	ENSP00000252490.5:p.Thr86=
ENST00000252490.5:c.258A>G (APOC4-APOC2)	ENSP00000252490.4:p.Thr86=
ENST00000585685.5:c.*1041A>G (APOC4-APOC2)	ENSP00000467185.1:n.*1041A>G
ENST00000585786.1:c.*337A>G (APOC2)	ENSP00000465001.1:n.*337A>G
ENST00000589057.5:c.489A>G (APOC4-APOC2)	ENSP00000468139.1:p.Thr163=
ENST00000590360.2:c.258A>G (APOC2)	ENSP00000466775.1:p.Thr86=
ENST00000591597.5:c.216A>G (APOC2)	ENSP00000476835.1:p.Thr72=
ENST00000592257.5:c.*52A>G (APOC2)	ENSP00000477261.1:n.*52A>G
NM_000483.4:c.258A>G (APOC2)	NP_000474.2:p.Thr86=
NR_037932.1:n.1465A>G (APOC4-APOC2)
NM_000483.5:c.258A>G (APOC2) MANE Select	NP_000474.2:p.Thr86=