Canonical Allele Identifier: CA476868925
Gene: APOC3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1782839
ClinVar RCV Id: RCV002410872
dbSNP Id: rs1179268663

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832776C>T , CM000673.2:g.116832776C>T GRCh38
NC_000011.9:g.116703492C>T , CM000673.1:g.116703492C>T GRCh37
NC_000011.8:g.116208702C>T NCBI36
NG_008949.1:g.7869C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.192C>T MANE Select ENSP00000227667.2:p.Thr64=
ENST00000227667.7:c.192C>T ENSP00000227667.2:p.Thr64=
ENST00000375345.3:c.246C>T ENSP00000364494.1:p.Thr82=
ENST00000630701.1:c.246C>T ENSP00000486182.1:p.Thr82=
NM_000040.1:c.192C>T NP_000031.1:p.Thr64=
NM_000040.2:c.192C>T NP_000031.1:p.Thr64=
NM_000040.3:c.192C>T MANE Select NP_000031.1:p.Thr64=