Canonical Allele Identifier: CA343320567

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192259C>T (hg19) ; chr1:g.161222469C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222469C>T , CM000663.2:g.161222469C>T	GRCh38
NC_000001.10:g.161192259C>T , CM000663.1:g.161192259C>T	GRCh37
NC_000001.9:g.159458883C>T	NCBI36
NG_012043.1:g.6160G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.239G>A MANE Select	ENSP00000356969.3:p.Gly80Glu
ENST00000463273.5:c.239G>A	ENSP00000476740.1:p.Gly80Glu
ENST00000463812.1:c.95G>A	ENSP00000476890.1:p.Gly32Glu
ENST00000464492.5:c.338G>A	ENSP00000476911.1:p.Gly113Glu
ENST00000468465.5:c.95G>A	ENSP00000476662.1:p.Gly32Glu
ENST00000470459.6:c.201-16G>A	ENSP00000477031.1:n.201-16G>A
ENST00000481413.1:n.750G>A
ENST00000481511.5:c.*236G>A	ENSP00000477054.1:n.*236G>A
ENST00000491350.1:c.*22G>A	ENSP00000477353.1:n.*22G>A
NM_001643.1:c.239G>A	NP_001634.1:p.Gly80Glu
NM_001643.2:c.239G>A MANE Select	NP_001634.1:p.Gly80Glu