Canonical Allele Identifier: CA2648766516

Gene: APOA2

Linked Data

• gnomAD v4: 1-161222598-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222598T>A , CM000663.2:g.161222598T>A	GRCh38
NC_000001.10:g.161192388T>A , CM000663.1:g.161192388T>A	GRCh37
NC_000001.9:g.159459012T>A	NCBI36
NG_012043.1:g.6031A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.186-76A>T MANE Select	ENSP00000356969.3:n.186-76A>T
ENST00000463273.5:c.186-76A>T	ENSP00000476740.1:n.186-76A>T
ENST00000463812.1:c.42-76A>T	ENSP00000476890.1:n.42-76A>T
ENST00000464492.5:c.285-76A>T	ENSP00000476911.1:n.285-76A>T
ENST00000468465.5:c.42-76A>T	ENSP00000476662.1:n.42-76A>T
ENST00000469730.2:c.186-76A>T	ENSP00000476605.1:n.186-76A>T
ENST00000470459.6:c.186-76A>T	ENSP00000477031.1:n.186-76A>T
ENST00000481413.1:n.697-76A>T
ENST00000481511.5:c.*183-76A>T	ENSP00000477054.1:n.*183-76A>T
ENST00000491350.1:c.53-76A>T	ENSP00000477353.1:n.53-76A>T
NM_001643.1:c.186-76A>T	NP_001634.1:n.186-76A>T
NM_001643.2:c.186-76A>T MANE Select	NP_001634.1:n.186-76A>T