Canonical Allele Identifier: CA507796192

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v4: 19-44949163-T-C
• MyVariant Identifiers: chr19:g.45452420T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949163T>C , CM000681.2:g.44949163T>C	GRCh38
NC_000019.9:g.45452420T>C , CM000681.1:g.45452420T>C	GRCh37
NC_000019.8:g.50144260T>C	NCBI36
NG_008837.1:g.8178T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.220T>C (APOC2) MANE Select	ENSP00000252490.5:p.Leu74=
ENST00000252490.5:c.220T>C (APOC4-APOC2)	ENSP00000252490.4:p.Leu74=
ENST00000585685.5:c.*1003T>C (APOC4-APOC2)	ENSP00000467185.1:n.*1003T>C
ENST00000585786.1:c.*299T>C (APOC2)	ENSP00000465001.1:n.*299T>C
ENST00000589057.5:c.451T>C (APOC4-APOC2)	ENSP00000468139.1:p.Leu151=
ENST00000590360.2:c.220T>C (APOC2)	ENSP00000466775.1:p.Leu74=
ENST00000591597.5:c.178T>C (APOC2)	ENSP00000476835.1:p.Leu60=
ENST00000592257.5:c.*14T>C (APOC2)	ENSP00000477261.1:n.*14T>C
NM_000483.4:c.220T>C (APOC2)	NP_000474.2:p.Leu74=
NR_037932.1:n.1427T>C (APOC4-APOC2)
NM_000483.5:c.220T>C (APOC2) MANE Select	NP_000474.2:p.Leu74=