Canonical Allele Identifier: CA343320741

Gene: APOA2

Linked Data

• dbSNP Id: rs776287664
• MyVariant Identifiers: chr1:g.161192288C>T (hg19) ; chr1:g.161222498C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222498C>T , CM000663.2:g.161222498C>T	GRCh38
NC_000001.10:g.161192288C>T , CM000663.1:g.161192288C>T	GRCh37
NC_000001.9:g.159458912C>T	NCBI36
NG_012043.1:g.6131G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.210G>A MANE Select	ENSP00000356969.3:p.Glu70=
ENST00000463273.5:c.210G>A	ENSP00000476740.1:p.Glu70=
ENST00000463812.1:c.66G>A	ENSP00000476890.1:p.Glu22=
ENST00000464492.5:c.309G>A	ENSP00000476911.1:p.Glu103=
ENST00000468465.5:c.66G>A	ENSP00000476662.1:p.Glu22=
ENST00000470459.6:c.200+10G>A	ENSP00000477031.1:n.200+10G>A
ENST00000481413.1:n.721G>A
ENST00000481511.5:c.*207G>A	ENSP00000477054.1:n.*207G>A
ENST00000491350.1:c.77G>A	ENSP00000477353.1:p.Ser26Asn
NM_001643.1:c.210G>A	NP_001634.1:p.Glu70=
NM_001643.2:c.210G>A MANE Select	NP_001634.1:p.Glu70=