Canonical Allele Identifier: CA343320479

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192240G>T (hg19) ; chr1:g.161222450G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222450G>T , CM000663.2:g.161222450G>T	GRCh38
NC_000001.10:g.161192240G>T , CM000663.1:g.161192240G>T	GRCh37
NC_000001.9:g.159458864G>T	NCBI36
NG_012043.1:g.6179C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.258C>A MANE Select	ENSP00000356969.3:p.Phe86Leu
ENST00000463273.5:c.258C>A	ENSP00000476740.1:p.Phe86Leu
ENST00000463812.1:c.114C>A	ENSP00000476890.1:p.Phe38Leu
ENST00000464492.5:c.357C>A	ENSP00000476911.1:p.Phe119Leu
ENST00000468465.5:c.114C>A	ENSP00000476662.1:p.Phe38Leu
ENST00000470459.6:c.204C>A	ENSP00000477031.1:p.Phe68Leu
ENST00000481413.1:n.769C>A
ENST00000481511.5:c.*255C>A	ENSP00000477054.1:n.*255C>A
ENST00000491350.1:c.*41C>A	ENSP00000477353.1:n.*41C>A
NM_001643.1:c.258C>A	NP_001634.1:p.Phe86Leu
NM_001643.2:c.258C>A MANE Select	NP_001634.1:p.Phe86Leu