Canonical Allele Identifier: CA1202652325

Gene: APOA2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222452A= , CM000663.2:g.161222452A=	GRCh38
NC_000001.10:g.161192242A= , CM000663.1:g.161192242A=	GRCh37
NC_000001.9:g.159458866A=	NCBI36
NG_012043.1:g.6177T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.256T= MANE Select	ENSP00000356969.3:p.Phe86=
ENST00000463273.5:c.256T=	ENSP00000476740.1:p.Phe86=
ENST00000463812.1:c.112T=	ENSP00000476890.1:p.Phe38=
ENST00000464492.5:c.355T=	ENSP00000476911.1:p.Phe119=
ENST00000468465.5:c.112T=	ENSP00000476662.1:p.Phe38=
ENST00000470459.6:c.202T=	ENSP00000477031.1:p.Phe68=
ENST00000481413.1:n.767T=
ENST00000481511.5:c.*253T=	ENSP00000477054.1:n.*253T=
ENST00000491350.1:c.*39T=	ENSP00000477353.1:n.*39T=
NM_001643.1:c.256T=	NP_001634.1:p.Phe86=
NM_001643.2:c.256T= MANE Select	NP_001634.1:p.Phe86=