Canonical Allele Identifier: CA2002758806

Gene: APOC3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116830620C= , CM000673.2:g.116830620C=	GRCh38
NC_000011.9:g.116701336C= , CM000673.1:g.116701336C=	GRCh37
NC_000011.8:g.116206546C=	NCBI36
NG_008949.1:g.5713C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000227667.8:c.38C= MANE Select	ENSP00000227667.2:p.Ala13=
ENST00000227667.7:c.38C=	ENSP00000227667.2:p.Ala13=
ENST00000375345.3:c.92C=	ENSP00000364494.1:p.Ala31=
ENST00000433777.5:c.38C=	ENSP00000410614.1:p.Ala13=
ENST00000470144.1:n.70C=
ENST00000630701.1:c.92C=	ENSP00000486182.1:p.Ala31=
NM_000040.1:c.38C=	NP_000031.1:p.Ala13=
NM_000040.2:c.38C=	NP_000031.1:p.Ala13=
NM_000040.3:c.38C= MANE Select	NP_000031.1:p.Ala13=