Canonical Allele Identifier: CA2002760319

Gene: APOC3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116832879G= , CM000673.2:g.116832879G=	GRCh38
NC_000011.9:g.116703595G= , CM000673.1:g.116703595G=	GRCh37
NC_000011.8:g.116208805G=	NCBI36
NG_008949.1:g.7972G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227667.8:c.295G= MANE Select	ENSP00000227667.2:p.Ala99=
ENST00000227667.7:c.295G=	ENSP00000227667.2:p.Ala99=
ENST00000375345.3:c.349G=	ENSP00000364494.1:p.Ala117=
ENST00000630701.1:c.349G=	ENSP00000486182.1:p.Ala117=
NM_000040.1:c.295G=	NP_000031.1:p.Ala99=
NM_000040.2:c.295G=	NP_000031.1:p.Ala99=
NM_000040.3:c.295G= MANE Select	NP_000031.1:p.Ala99=