Canonical Allele Identifier: CA406295220

Gene: APOC2 APOC4-APOC2

Linked Data

• MyVariant Identifiers: chr19:g.45452442C>T (hg19) ; chr19:g.44949185C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949185C>T , CM000681.2:g.44949185C>T	GRCh38
NC_000019.9:g.45452442C>T , CM000681.1:g.45452442C>T	GRCh37
NC_000019.8:g.50144282C>T	NCBI36
NG_008837.1:g.8200C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252490.7:c.242C>T (APOC2) MANE Select	ENSP00000252490.5:p.Ala81Val
ENST00000252490.5:c.242C>T (APOC4-APOC2)	ENSP00000252490.4:p.Ala81Val
ENST00000585685.5:c.*1025C>T (APOC4-APOC2)	ENSP00000467185.1:n.*1025C>T
ENST00000585786.1:c.*321C>T (APOC2)	ENSP00000465001.1:n.*321C>T
ENST00000589057.5:c.473C>T (APOC4-APOC2)	ENSP00000468139.1:p.Ala158Val
ENST00000590360.2:c.242C>T (APOC2)	ENSP00000466775.1:p.Ala81Val
ENST00000591597.5:c.200C>T (APOC2)	ENSP00000476835.1:p.Ala67Val
ENST00000592257.5:c.*36C>T (APOC2)	ENSP00000477261.1:n.*36C>T
NM_000483.4:c.242C>T (APOC2)	NP_000474.2:p.Ala81Val
NR_037932.1:n.1449C>T (APOC4-APOC2)
NM_000483.5:c.242C>T (APOC2) MANE Select	NP_000474.2:p.Ala81Val