Canonical Allele Identifier: CA6289616
Gene: APOC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1736872
ClinVar RCV Id: RCV002357797
dbSNP Id: rs762766868

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830621G>A , CM000673.2:g.116830621G>A GRCh38
NC_000011.9:g.116701337G>A , CM000673.1:g.116701337G>A GRCh37
NC_000011.8:g.116206547G>A NCBI36
NG_008949.1:g.5714G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.39G>A MANE Select ENSP00000227667.2:p.Ala13=
ENST00000227667.7:c.39G>A ENSP00000227667.2:p.Ala13=
ENST00000375345.3:c.93G>A ENSP00000364494.1:p.Ala31=
ENST00000433777.5:c.39G>A ENSP00000410614.1:p.Ala13=
ENST00000470144.1:n.71G>A
ENST00000630701.1:c.93G>A ENSP00000486182.1:p.Ala31=
NM_000040.1:c.39G>A NP_000031.1:p.Ala13=
NM_000040.2:c.39G>A NP_000031.1:p.Ala13=
NM_000040.3:c.39G>A MANE Select NP_000031.1:p.Ala13=