Canonical Allele Identifier: CA507796198

Gene: APOC2 APOC4-APOC2

Linked Data

• MyVariant Identifiers: chr19:g.45452434C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949177C>T , CM000681.2:g.44949177C>T	GRCh38
NC_000019.9:g.45452434C>T , CM000681.1:g.45452434C>T	GRCh37
NC_000019.8:g.50144274C>T	NCBI36
NG_008837.1:g.8192C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.234C>T (APOC2) MANE Select	ENSP00000252490.5:p.Ser78=
ENST00000252490.5:c.234C>T (APOC4-APOC2)	ENSP00000252490.4:p.Ser78=
ENST00000585685.5:c.*1017C>T (APOC4-APOC2)	ENSP00000467185.1:n.*1017C>T
ENST00000585786.1:c.*313C>T (APOC2)	ENSP00000465001.1:n.*313C>T
ENST00000589057.5:c.465C>T (APOC4-APOC2)	ENSP00000468139.1:p.Ser155=
ENST00000590360.2:c.234C>T (APOC2)	ENSP00000466775.1:p.Ser78=
ENST00000591597.5:c.192C>T (APOC2)	ENSP00000476835.1:p.Ser64=
ENST00000592257.5:c.*28C>T (APOC2)	ENSP00000477261.1:n.*28C>T
NM_000483.4:c.234C>T (APOC2)	NP_000474.2:p.Ser78=
NR_037932.1:n.1441C>T (APOC4-APOC2)
NM_000483.5:c.234C>T (APOC2) MANE Select	NP_000474.2:p.Ser78=