Canonical Allele Identifier: CA1202652277

Gene: APOA2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222340C= , CM000663.2:g.161222340C=	GRCh38
NC_000001.10:g.161192130C= , CM000663.1:g.161192130C=	GRCh37
NC_000001.9:g.159458754C=	NCBI36
NG_012043.1:g.6289G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.*65G= MANE Select	ENSP00000356969.3:n.*65G=
ENST00000463812.1:c.*65G=	ENSP00000476890.1:n.*65G=
ENST00000464492.5:c.*65G=	ENSP00000476911.1:n.*65G=
ENST00000468465.5:c.*65G=	ENSP00000476662.1:n.*65G=
ENST00000470459.6:c.*65G=	ENSP00000477031.1:n.*65G=
ENST00000481413.1:n.879G=
ENST00000481511.5:c.*365G=	ENSP00000477054.1:n.*365G=
ENST00000491350.1:c.*151G=	ENSP00000477353.1:n.*151G=
NM_001643.1:c.*65G=	NP_001634.1:n.*65G=
NM_001643.2:c.*65G= MANE Select	NP_001634.1:n.*65G=