Canonical Allele Identifier: CA421400176

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192132C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222342C>A , CM000663.2:g.161222342C>A	GRCh38
NC_000001.10:g.161192132C>A , CM000663.1:g.161192132C>A	GRCh37
NC_000001.9:g.159458756C>A	NCBI36
NG_012043.1:g.6287G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.*63G>T MANE Select	ENSP00000356969.3:n.*63G>T
ENST00000463812.1:c.*63G>T	ENSP00000476890.1:n.*63G>T
ENST00000464492.5:c.*63G>T	ENSP00000476911.1:n.*63G>T
ENST00000468465.5:c.*63G>T	ENSP00000476662.1:n.*63G>T
ENST00000470459.6:c.*63G>T	ENSP00000477031.1:n.*63G>T
ENST00000481413.1:n.877G>T
ENST00000481511.5:c.*363G>T	ENSP00000477054.1:n.*363G>T
ENST00000491350.1:c.*149G>T	ENSP00000477353.1:n.*149G>T
NM_001643.1:c.*63G>T	NP_001634.1:n.*63G>T
NM_001643.2:c.*63G>T MANE Select	NP_001634.1:n.*63G>T