Canonical Allele Identifier: CA406295396

Gene: APOC2 APOC4-APOC2

Linked Data

• gnomAD v4: 19-44949214-G-T
• MyVariant Identifiers: chr19:g.45452471G>T (hg19) ; chr19:g.44949214G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44949214G>T , CM000681.2:g.44949214G>T	GRCh38
NC_000019.9:g.45452471G>T , CM000681.1:g.45452471G>T	GRCh37
NC_000019.8:g.50144311G>T	NCBI36
NG_008837.1:g.8229G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252490.7:c.271G>T (APOC2) MANE Select	ENSP00000252490.5:p.Asp91Tyr
ENST00000252490.5:c.271G>T (APOC4-APOC2)	ENSP00000252490.4:p.Asp91Tyr
ENST00000585685.5:c.*1054G>T (APOC4-APOC2)	ENSP00000467185.1:n.*1054G>T
ENST00000585786.1:c.*350G>T (APOC2)	ENSP00000465001.1:n.*350G>T
ENST00000589057.5:c.502G>T (APOC4-APOC2)	ENSP00000468139.1:p.Asp168Tyr
ENST00000590360.2:c.271G>T (APOC2)	ENSP00000466775.1:p.Asp91Tyr
ENST00000591597.5:c.229G>T (APOC2)	ENSP00000476835.1:p.Asp77Tyr
ENST00000592257.5:c.*65G>T (APOC2)	ENSP00000477261.1:n.*65G>T
NM_000483.4:c.271G>T (APOC2)	NP_000474.2:p.Asp91Tyr
NR_037932.1:n.1478G>T (APOC4-APOC2)
NM_000483.5:c.271G>T (APOC2) MANE Select	NP_000474.2:p.Asp91Tyr