Canonical Allele Identifier: CA2002758814
Gene: APOC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830637C= , CM000673.2:g.116830637C= GRCh38
NC_000011.9:g.116701353C= , CM000673.1:g.116701353C= GRCh37
NC_000011.8:g.116206563C= NCBI36
NG_008949.1:g.5730C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.55C= MANE Select ENSP00000227667.2:p.Arg19=
ENST00000227667.7:c.55C= ENSP00000227667.2:p.Arg19=
ENST00000375345.3:c.109C= ENSP00000364494.1:p.Arg37=
ENST00000433777.5:c.55C= ENSP00000410614.1:p.Arg19=
ENST00000470144.1:n.87C=
ENST00000630701.1:c.109C= ENSP00000486182.1:p.Arg37=
NM_000040.1:c.55C= NP_000031.1:p.Arg19=
NM_000040.2:c.55C= NP_000031.1:p.Arg19=
NM_000040.3:c.55C= MANE Select NP_000031.1:p.Arg19=