Canonical Allele Identifier: CA2002760315
Gene: APOC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832871C= , CM000673.2:g.116832871C= GRCh38
NC_000011.9:g.116703587C= , CM000673.1:g.116703587C= GRCh37
NC_000011.8:g.116208797C= NCBI36
NG_008949.1:g.7964C=

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.287C= MANE Select ENSP00000227667.2:p.Ala96=
ENST00000227667.7:c.287C= ENSP00000227667.2:p.Ala96=
ENST00000375345.3:c.341C= ENSP00000364494.1:p.Ala114=
ENST00000630701.1:c.341C= ENSP00000486182.1:p.Ala114=
NM_000040.1:c.287C= NP_000031.1:p.Ala96=
NM_000040.2:c.287C= NP_000031.1:p.Ala96=
NM_000040.3:c.287C= MANE Select NP_000031.1:p.Ala96=