Canonical Allele Identifier: CA2002760232

Gene: APOC3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116832699G= , CM000673.2:g.116832699G=	GRCh38
NC_000011.9:g.116703415G= , CM000673.1:g.116703415G=	GRCh37
NC_000011.8:g.116208625G=	NCBI36
NG_008949.1:g.7792G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227667.8:c.180-65G= MANE Select	ENSP00000227667.2:n.180-65G=
ENST00000227667.7:c.180-65G=	ENSP00000227667.2:n.180-65G=
ENST00000375345.3:c.234-65G=	ENSP00000364494.1:n.234-65G=
ENST00000630701.1:c.234-65G=	ENSP00000486182.1:n.234-65G=
NM_000040.1:c.180-65G=	NP_000031.1:n.180-65G=
NM_000040.2:c.180-65G=	NP_000031.1:n.180-65G=
NM_000040.3:c.180-65G= MANE Select	NP_000031.1:n.180-65G=