Canonical Allele Identifier: CA2002758807
Gene: APOC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830621G= , CM000673.2:g.116830621G= GRCh38
NC_000011.9:g.116701337G= , CM000673.1:g.116701337G= GRCh37
NC_000011.8:g.116206547G= NCBI36
NG_008949.1:g.5714G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.39G= MANE Select ENSP00000227667.2:p.Ala13=
ENST00000227667.7:c.39G= ENSP00000227667.2:p.Ala13=
ENST00000375345.3:c.93G= ENSP00000364494.1:p.Ala31=
ENST00000433777.5:c.39G= ENSP00000410614.1:p.Ala13=
ENST00000470144.1:n.71G=
ENST00000630701.1:c.93G= ENSP00000486182.1:p.Ala31=
NM_000040.1:c.39G= NP_000031.1:p.Ala13=
NM_000040.2:c.39G= NP_000031.1:p.Ala13=
NM_000040.3:c.39G= MANE Select NP_000031.1:p.Ala13=