Canonical Allele Identifier: CA1202652282

Gene: APOA2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222346G= , CM000663.2:g.161222346G=	GRCh38
NC_000001.10:g.161192136G= , CM000663.1:g.161192136G=	GRCh37
NC_000001.9:g.159458760G=	NCBI36
NG_012043.1:g.6283C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.*59C= MANE Select	ENSP00000356969.3:n.*59C=
ENST00000463812.1:c.*59C=	ENSP00000476890.1:n.*59C=
ENST00000464492.5:c.*59C=	ENSP00000476911.1:n.*59C=
ENST00000468465.5:c.*59C=	ENSP00000476662.1:n.*59C=
ENST00000470459.6:c.*59C=	ENSP00000477031.1:n.*59C=
ENST00000481413.1:n.873C=
ENST00000481511.5:c.*359C=	ENSP00000477054.1:n.*359C=
ENST00000491350.1:c.*145C=	ENSP00000477353.1:n.*145C=
NM_001643.1:c.*59C=	NP_001634.1:n.*59C=
NM_001643.2:c.*59C= MANE Select	NP_001634.1:n.*59C=