Canonical Allele Identifier: CA421401085

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192222T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222432T>C , CM000663.2:g.161222432T>C	GRCh38
NC_000001.10:g.161192222T>C , CM000663.1:g.161192222T>C	GRCh37
NC_000001.9:g.159458846T>C	NCBI36
NG_012043.1:g.6197A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.276A>G MANE Select	ENSP00000356969.3:p.Glu92=
ENST00000463273.5:c.276A>G	ENSP00000476740.1:p.Glu92=
ENST00000463812.1:c.132A>G	ENSP00000476890.1:p.Glu44=
ENST00000464492.5:c.375A>G	ENSP00000476911.1:p.Glu125=
ENST00000468465.5:c.132A>G	ENSP00000476662.1:p.Glu44=
ENST00000470459.6:c.222A>G	ENSP00000477031.1:p.Glu74=
ENST00000481413.1:n.787A>G
ENST00000481511.5:c.*273A>G	ENSP00000477054.1:n.*273A>G
ENST00000491350.1:c.*59A>G	ENSP00000477353.1:n.*59A>G
NM_001643.1:c.276A>G	NP_001634.1:p.Glu92=
NM_001643.2:c.276A>G MANE Select	NP_001634.1:p.Glu92=