Canonical Allele Identifier: CA1202652279

Gene: APOA2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222343T= , CM000663.2:g.161222343T=	GRCh38
NC_000001.10:g.161192133T= , CM000663.1:g.161192133T=	GRCh37
NC_000001.9:g.159458757T=	NCBI36
NG_012043.1:g.6286A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.*62A= MANE Select	ENSP00000356969.3:n.*62A=
ENST00000463812.1:c.*62A=	ENSP00000476890.1:n.*62A=
ENST00000464492.5:c.*62A=	ENSP00000476911.1:n.*62A=
ENST00000468465.5:c.*62A=	ENSP00000476662.1:n.*62A=
ENST00000470459.6:c.*62A=	ENSP00000477031.1:n.*62A=
ENST00000481413.1:n.876A=
ENST00000481511.5:c.*362A=	ENSP00000477054.1:n.*362A=
ENST00000491350.1:c.*148A=	ENSP00000477353.1:n.*148A=
NM_001643.1:c.*62A=	NP_001634.1:n.*62A=
NM_001643.2:c.*62A= MANE Select	NP_001634.1:n.*62A=