Canonical Allele Identifier: CA1630855356
Gene: APOC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830819T= , CM000673.2:g.116830819T= GRCh38
NC_000011.9:g.116701535T= , CM000673.1:g.116701535T= GRCh37
NC_000011.8:g.116206745T= NCBI36
NG_008949.1:g.5912T=

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.102T= MANE Select ENSP00000227667.2:p.Gly34=
ENST00000227667.7:c.102T= ENSP00000227667.2:p.Gly34=
ENST00000375345.3:c.156T= ENSP00000364494.1:p.Gly52=
ENST00000433777.5:c.102T= ENSP00000410614.1:p.Gly34=
ENST00000470144.1:n.134T=
ENST00000630701.1:c.156T= ENSP00000486182.1:p.Gly52=
NM_000040.1:c.102T= NP_000031.1:p.Gly34=
NM_000040.2:c.102T= NP_000031.1:p.Gly34=
NM_000040.3:c.102T= MANE Select NP_000031.1:p.Gly34=