Canonical Allele Identifier: CA343320375

Gene: APOA2

Linked Data

• dbSNP Id: rs1288140955
• gnomAD v4: 1-161222424-G-T
• MyVariant Identifiers: chr1:g.161192214G>T (hg19) ; chr1:g.161222424G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222424G>T , CM000663.2:g.161222424G>T	GRCh38
NC_000001.10:g.161192214G>T , CM000663.1:g.161192214G>T	GRCh37
NC_000001.9:g.159458838G>T	NCBI36
NG_012043.1:g.6205C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.284C>A MANE Select	ENSP00000356969.3:p.Thr95Lys
ENST00000463273.5:c.284C>A	ENSP00000476740.1:p.Thr95Lys
ENST00000463812.1:c.140C>A	ENSP00000476890.1:p.Thr47Lys
ENST00000464492.5:c.383C>A	ENSP00000476911.1:p.Thr128Lys
ENST00000468465.5:c.140C>A	ENSP00000476662.1:p.Thr47Lys
ENST00000470459.6:c.230C>A	ENSP00000477031.1:p.Thr77Lys
ENST00000481413.1:n.795C>A
ENST00000481511.5:c.*281C>A	ENSP00000477054.1:n.*281C>A
ENST00000491350.1:c.*67C>A	ENSP00000477353.1:n.*67C>A
NM_001643.1:c.284C>A	NP_001634.1:p.Thr95Lys
NM_001643.2:c.284C>A MANE Select	NP_001634.1:p.Thr95Lys