Canonical Allele Identifier: CA421400224

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192138C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222348C>A , CM000663.2:g.161222348C>A	GRCh38
NC_000001.10:g.161192138C>A , CM000663.1:g.161192138C>A	GRCh37
NC_000001.9:g.159458762C>A	NCBI36
NG_012043.1:g.6281G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.*57G>T MANE Select	ENSP00000356969.3:n.*57G>T
ENST00000463812.1:c.*57G>T	ENSP00000476890.1:n.*57G>T
ENST00000464492.5:c.*57G>T	ENSP00000476911.1:n.*57G>T
ENST00000468465.5:c.*57G>T	ENSP00000476662.1:n.*57G>T
ENST00000470459.6:c.*57G>T	ENSP00000477031.1:n.*57G>T
ENST00000481413.1:n.871G>T
ENST00000481511.5:c.*357G>T	ENSP00000477054.1:n.*357G>T
ENST00000491350.1:c.*143G>T	ENSP00000477353.1:n.*143G>T
NM_001643.1:c.*57G>T	NP_001634.1:n.*57G>T
NM_001643.2:c.*57G>T MANE Select	NP_001634.1:n.*57G>T