Canonical Allele Identifier: CA1202652272

Gene: APOA2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222331G= , CM000663.2:g.161222331G=	GRCh38
NC_000001.10:g.161192121G= , CM000663.1:g.161192121G=	GRCh37
NC_000001.9:g.159458745G=	NCBI36
NG_012043.1:g.6298C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.*74C= MANE Select	ENSP00000356969.3:n.*74C=
ENST00000463812.1:c.*74C=	ENSP00000476890.1:n.*74C=
ENST00000464492.5:c.*74C=	ENSP00000476911.1:n.*74C=
ENST00000468465.5:c.*74C=	ENSP00000476662.1:n.*74C=
ENST00000470459.6:c.*74C=	ENSP00000477031.1:n.*74C=
ENST00000481413.1:n.888C=
ENST00000481511.5:c.*374C=	ENSP00000477054.1:n.*374C=
ENST00000491350.1:c.*160C=	ENSP00000477353.1:n.*160C=
NM_001643.1:c.*74C=	NP_001634.1:n.*74C=
NM_001643.2:c.*74C= MANE Select	NP_001634.1:n.*74C=