Canonical Allele Identifier: CA2002758826

Gene: APOC3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116830654A= , CM000673.2:g.116830654A=	GRCh38
NC_000011.9:g.116701370A= , CM000673.1:g.116701370A=	GRCh37
NC_000011.8:g.116206580A=	NCBI36
NG_008949.1:g.5747A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000227667.8:c.55+17A= MANE Select	ENSP00000227667.2:n.55+17A=
ENST00000227667.7:c.55+17A=	ENSP00000227667.2:n.55+17A=
ENST00000375345.3:c.109+17A=	ENSP00000364494.1:n.109+17A=
ENST00000433777.5:c.55+17A=	ENSP00000410614.1:n.55+17A=
ENST00000470144.1:n.87+17A=
ENST00000630701.1:c.109+17A=	ENSP00000486182.1:n.109+17A=
NM_000040.1:c.55+17A=	NP_000031.1:n.55+17A=
NM_000040.2:c.55+17A=	NP_000031.1:n.55+17A=
NM_000040.3:c.55+17A= MANE Select	NP_000031.1:n.55+17A=