Canonical Allele Identifier: CA507796191

Gene: APOC2 APOC4-APOC2

Linked Data

• MyVariant Identifiers: chr19:g.45452419C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949162C>T , CM000681.2:g.44949162C>T	GRCh38
NC_000019.9:g.45452419C>T , CM000681.1:g.45452419C>T	GRCh37
NC_000019.8:g.50144259C>T	NCBI36
NG_008837.1:g.8177C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.219C>T (APOC2) MANE Select	ENSP00000252490.5:p.Asp73=
ENST00000252490.5:c.219C>T (APOC4-APOC2)	ENSP00000252490.4:p.Asp73=
ENST00000585685.5:c.*1002C>T (APOC4-APOC2)	ENSP00000467185.1:n.*1002C>T
ENST00000585786.1:c.*298C>T (APOC2)	ENSP00000465001.1:n.*298C>T
ENST00000589057.5:c.450C>T (APOC4-APOC2)	ENSP00000468139.1:p.Asp150=
ENST00000590360.2:c.219C>T (APOC2)	ENSP00000466775.1:p.Asp73=
ENST00000591597.5:c.177C>T (APOC2)	ENSP00000476835.1:p.Asp59=
ENST00000592257.5:c.*13C>T (APOC2)	ENSP00000477261.1:n.*13C>T
NM_000483.4:c.219C>T (APOC2)	NP_000474.2:p.Asp73=
NR_037932.1:n.1426C>T (APOC4-APOC2)
NM_000483.5:c.219C>T (APOC2) MANE Select	NP_000474.2:p.Asp73=