Canonical Allele Identifier: CA343320413

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192224C>A (hg19) ; chr1:g.161222434C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222434C>A , CM000663.2:g.161222434C>A	GRCh38
NC_000001.10:g.161192224C>A , CM000663.1:g.161192224C>A	GRCh37
NC_000001.9:g.159458848C>A	NCBI36
NG_012043.1:g.6195G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.274G>T MANE Select	ENSP00000356969.3:p.Glu92Ter
ENST00000463273.5:c.274G>T	ENSP00000476740.1:p.Glu92Ter
ENST00000463812.1:c.130G>T	ENSP00000476890.1:p.Glu44Ter
ENST00000464492.5:c.373G>T	ENSP00000476911.1:p.Glu125Ter
ENST00000468465.5:c.130G>T	ENSP00000476662.1:p.Glu44Ter
ENST00000470459.6:c.220G>T	ENSP00000477031.1:p.Glu74Ter
ENST00000481413.1:n.785G>T
ENST00000481511.5:c.*271G>T	ENSP00000477054.1:n.*271G>T
ENST00000491350.1:c.*57G>T	ENSP00000477353.1:n.*57G>T
NM_001643.1:c.274G>T	NP_001634.1:p.Glu92Ter
NM_001643.2:c.274G>T MANE Select	NP_001634.1:p.Glu92Ter