Canonical Allele Identifier: CA343320476

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192239A>T (hg19) ; chr1:g.161222449A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222449A>T , CM000663.2:g.161222449A>T	GRCh38
NC_000001.10:g.161192239A>T , CM000663.1:g.161192239A>T	GRCh37
NC_000001.9:g.159458863A>T	NCBI36
NG_012043.1:g.6180T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.259T>A MANE Select	ENSP00000356969.3:p.Leu87Met
ENST00000463273.5:c.259T>A	ENSP00000476740.1:p.Leu87Met
ENST00000463812.1:c.115T>A	ENSP00000476890.1:p.Leu39Met
ENST00000464492.5:c.358T>A	ENSP00000476911.1:p.Leu120Met
ENST00000468465.5:c.115T>A	ENSP00000476662.1:p.Leu39Met
ENST00000470459.6:c.205T>A	ENSP00000477031.1:p.Leu69Met
ENST00000481413.1:n.770T>A
ENST00000481511.5:c.*256T>A	ENSP00000477054.1:n.*256T>A
ENST00000491350.1:c.*42T>A	ENSP00000477353.1:n.*42T>A
NM_001643.1:c.259T>A	NP_001634.1:p.Leu87Met
NM_001643.2:c.259T>A MANE Select	NP_001634.1:p.Leu87Met