Canonical Allele Identifier: CA2002760305
Gene: APOC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832848C= , CM000673.2:g.116832848C= GRCh38
NC_000011.9:g.116703564C= , CM000673.1:g.116703564C= GRCh37
NC_000011.8:g.116208774C= NCBI36
NG_008949.1:g.7941C=

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.264C= MANE Select ENSP00000227667.2:p.Asp88=
ENST00000227667.7:c.264C= ENSP00000227667.2:p.Asp88=
ENST00000375345.3:c.318C= ENSP00000364494.1:p.Asp106=
ENST00000630701.1:c.318C= ENSP00000486182.1:p.Asp106=
NM_000040.1:c.264C= NP_000031.1:p.Asp88=
NM_000040.2:c.264C= NP_000031.1:p.Asp88=
NM_000040.3:c.264C= MANE Select NP_000031.1:p.Asp88=