Canonical Allele Identifier: CA382711129
Gene: APOC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116703495T>A (hg19) chr11:g.116832779T>A (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.195T>A MANE Select ENSP00000227667.2:p.Asp65Glu
ENST00000227667.7:c.195T>A ENSP00000227667.2:p.Asp65Glu
ENST00000375345.3:c.249T>A ENSP00000364494.1:p.Asp83Glu
ENST00000630701.1:c.249T>A ENSP00000486182.1:p.Asp83Glu
NM_000040.1:c.195T>A NP_000031.1:p.Asp65Glu
NM_000040.2:c.195T>A NP_000031.1:p.Asp65Glu
NM_000040.3:c.195T>A MANE Select NP_000031.1:p.Asp65Glu
Search 100 bp 5'
Search 100 bp 3'