Canonical Allele Identifier: CA2002758828

Gene: APOC3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116830659G= , CM000673.2:g.116830659G=	GRCh38
NC_000011.9:g.116701375G= , CM000673.1:g.116701375G=	GRCh37
NC_000011.8:g.116206585G=	NCBI36
NG_008949.1:g.5752G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000227667.8:c.55+22G= MANE Select	ENSP00000227667.2:n.55+22G=
ENST00000227667.7:c.55+22G=	ENSP00000227667.2:n.55+22G=
ENST00000375345.3:c.109+22G=	ENSP00000364494.1:n.109+22G=
ENST00000433777.5:c.55+22G=	ENSP00000410614.1:n.55+22G=
ENST00000470144.1:n.87+22G=
ENST00000630701.1:c.109+22G=	ENSP00000486182.1:n.109+22G=
NM_000040.1:c.55+22G=	NP_000031.1:n.55+22G=
NM_000040.2:c.55+22G=	NP_000031.1:n.55+22G=
NM_000040.3:c.55+22G= MANE Select	NP_000031.1:n.55+22G=