Canonical Allele Identifier: CA406295028

Gene: APOC2 APOC4-APOC2

Linked Data

• MyVariant Identifiers: chr19:g.45452416G>T (hg19) ; chr19:g.44949159G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949159G>T , CM000681.2:g.44949159G>T	GRCh38
NC_000019.9:g.45452416G>T , CM000681.1:g.45452416G>T	GRCh37
NC_000019.8:g.50144256G>T	NCBI36
NG_008837.1:g.8174G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.216G>T (APOC2) MANE Select	ENSP00000252490.5:p.Arg72Ser
ENST00000252490.5:c.216G>T (APOC4-APOC2)	ENSP00000252490.4:p.Arg72Ser
ENST00000585685.5:c.*999G>T (APOC4-APOC2)	ENSP00000467185.1:n.*999G>T
ENST00000585786.1:c.*295G>T (APOC2)	ENSP00000465001.1:n.*295G>T
ENST00000589057.5:c.447G>T (APOC4-APOC2)	ENSP00000468139.1:p.Arg149Ser
ENST00000590360.2:c.216G>T (APOC2)	ENSP00000466775.1:p.Arg72Ser
ENST00000591597.5:c.174G>T (APOC2)	ENSP00000476835.1:p.Leu58=
ENST00000592257.5:c.*10G>T (APOC2)	ENSP00000477261.1:n.*10G>T
NM_000483.4:c.216G>T (APOC2)	NP_000474.2:p.Arg72Ser
NR_037932.1:n.1423G>T (APOC4-APOC2)
NM_000483.5:c.216G>T (APOC2) MANE Select	NP_000474.2:p.Arg72Ser