Canonical Allele Identifier: CA421400232

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192139T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222349T>A , CM000663.2:g.161222349T>A	GRCh38
NC_000001.10:g.161192139T>A , CM000663.1:g.161192139T>A	GRCh37
NC_000001.9:g.159458763T>A	NCBI36
NG_012043.1:g.6280A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.*56A>T MANE Select	ENSP00000356969.3:n.*56A>T
ENST00000463812.1:c.*56A>T	ENSP00000476890.1:n.*56A>T
ENST00000464492.5:c.*56A>T	ENSP00000476911.1:n.*56A>T
ENST00000468465.5:c.*56A>T	ENSP00000476662.1:n.*56A>T
ENST00000470459.6:c.*56A>T	ENSP00000477031.1:n.*56A>T
ENST00000481413.1:n.870A>T
ENST00000481511.5:c.*356A>T	ENSP00000477054.1:n.*356A>T
ENST00000491350.1:c.*142A>T	ENSP00000477353.1:n.*142A>T
NM_001643.1:c.*56A>T	NP_001634.1:n.*56A>T
NM_001643.2:c.*56A>T MANE Select	NP_001634.1:n.*56A>T