Canonical Allele Identifier: CA2002758877
Gene: APOC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830742T= , CM000673.2:g.116830742T= GRCh38
NC_000011.9:g.116701458T= , CM000673.1:g.116701458T= GRCh37
NC_000011.8:g.116206668T= NCBI36
NG_008949.1:g.5835T=

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.56-31T= MANE Select ENSP00000227667.2:n.56-31T=
ENST00000227667.7:c.56-31T= ENSP00000227667.2:n.56-31T=
ENST00000375345.3:c.110-31T= ENSP00000364494.1:n.110-31T=
ENST00000433777.5:c.56-31T= ENSP00000410614.1:n.56-31T=
ENST00000470144.1:n.88-31T=
ENST00000630701.1:c.110-31T= ENSP00000486182.1:n.110-31T=
NM_000040.1:c.56-31T= NP_000031.1:n.56-31T=
NM_000040.2:c.56-31T= NP_000031.1:n.56-31T=
NM_000040.3:c.56-31T= MANE Select NP_000031.1:n.56-31T=