Canonical Allele Identifier: CA382711483
Gene: APOC3 HGNC NCBI

Linked Data

COSMIC: COSM386465

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832837T>A , CM000673.2:g.116832837T>A GRCh38
NC_000011.9:g.116703553T>A , CM000673.1:g.116703553T>A GRCh37
NC_000011.8:g.116208763T>A NCBI36
NG_008949.1:g.7930T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.253T>A MANE Select ENSP00000227667.2:p.Trp85Arg
ENST00000227667.7:c.253T>A ENSP00000227667.2:p.Trp85Arg
ENST00000375345.3:c.307T>A ENSP00000364494.1:p.Trp103Arg
ENST00000630701.1:c.307T>A ENSP00000486182.1:p.Trp103Arg
NM_000040.1:c.253T>A NP_000031.1:p.Trp85Arg
NM_000040.2:c.253T>A NP_000031.1:p.Trp85Arg
NM_000040.3:c.253T>A MANE Select NP_000031.1:p.Trp85Arg