Canonical Allele Identifier: CA507796210

Gene: APOC2 APOC4-APOC2

Linked Data

• MyVariant Identifiers: chr19:g.45452452T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949195T>C , CM000681.2:g.44949195T>C	GRCh38
NC_000019.9:g.45452452T>C , CM000681.1:g.45452452T>C	GRCh37
NC_000019.8:g.50144292T>C	NCBI36
NG_008837.1:g.8210T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.252T>C (APOC2) MANE Select	ENSP00000252490.5:p.Thr84=
ENST00000252490.5:c.252T>C (APOC4-APOC2)	ENSP00000252490.4:p.Thr84=
ENST00000585685.5:c.*1035T>C (APOC4-APOC2)	ENSP00000467185.1:n.*1035T>C
ENST00000585786.1:c.*331T>C (APOC2)	ENSP00000465001.1:n.*331T>C
ENST00000589057.5:c.483T>C (APOC4-APOC2)	ENSP00000468139.1:p.Thr161=
ENST00000590360.2:c.252T>C (APOC2)	ENSP00000466775.1:p.Thr84=
ENST00000591597.5:c.210T>C (APOC2)	ENSP00000476835.1:p.Thr70=
ENST00000592257.5:c.*46T>C (APOC2)	ENSP00000477261.1:n.*46T>C
NM_000483.4:c.252T>C (APOC2)	NP_000474.2:p.Thr84=
NR_037932.1:n.1459T>C (APOC4-APOC2)
NM_000483.5:c.252T>C (APOC2) MANE Select	NP_000474.2:p.Thr84=