Canonical Allele Identifier: CA229320860
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs772255301

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832779T>C , CM000673.2:g.116832779T>C GRCh38
NC_000011.9:g.116703495T>C , CM000673.1:g.116703495T>C GRCh37
NC_000011.8:g.116208705T>C NCBI36
NG_008949.1:g.7872T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.195T>C MANE Select ENSP00000227667.2:p.Asp65=
ENST00000227667.7:c.195T>C ENSP00000227667.2:p.Asp65=
ENST00000375345.3:c.249T>C ENSP00000364494.1:p.Asp83=
ENST00000630701.1:c.249T>C ENSP00000486182.1:p.Asp83=
NM_000040.1:c.195T>C NP_000031.1:p.Asp65=
NM_000040.2:c.195T>C NP_000031.1:p.Asp65=
NM_000040.3:c.195T>C MANE Select NP_000031.1:p.Asp65=