Canonical Allele Identifier: CA2002758813
Gene: APOC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830635C= , CM000673.2:g.116830635C= GRCh38
NC_000011.9:g.116701351C= , CM000673.1:g.116701351C= GRCh37
NC_000011.8:g.116206561C= NCBI36
NG_008949.1:g.5728C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.53C= MANE Select ENSP00000227667.2:p.Ala18=
ENST00000227667.7:c.53C= ENSP00000227667.2:p.Ala18=
ENST00000375345.3:c.107C= ENSP00000364494.1:p.Ala36=
ENST00000433777.5:c.53C= ENSP00000410614.1:p.Ala18=
ENST00000470144.1:n.85C=
ENST00000630701.1:c.107C= ENSP00000486182.1:p.Ala36=
NM_000040.1:c.53C= NP_000031.1:p.Ala18=
NM_000040.2:c.53C= NP_000031.1:p.Ala18=
NM_000040.3:c.53C= MANE Select NP_000031.1:p.Ala18=