Canonical Allele Identifier: CA421401114

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192225C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222435C>T , CM000663.2:g.161222435C>T	GRCh38
NC_000001.10:g.161192225C>T , CM000663.1:g.161192225C>T	GRCh37
NC_000001.9:g.159458849C>T	NCBI36
NG_012043.1:g.6194G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.273G>A MANE Select	ENSP00000356969.3:p.Val91=
ENST00000463273.5:c.273G>A	ENSP00000476740.1:p.Val91=
ENST00000463812.1:c.129G>A	ENSP00000476890.1:p.Val43=
ENST00000464492.5:c.372G>A	ENSP00000476911.1:p.Val124=
ENST00000468465.5:c.129G>A	ENSP00000476662.1:p.Val43=
ENST00000470459.6:c.219G>A	ENSP00000477031.1:p.Val73=
ENST00000481413.1:n.784G>A
ENST00000481511.5:c.*270G>A	ENSP00000477054.1:n.*270G>A
ENST00000491350.1:c.*56G>A	ENSP00000477353.1:n.*56G>A
NM_001643.1:c.273G>A	NP_001634.1:p.Val91=
NM_001643.2:c.273G>A MANE Select	NP_001634.1:p.Val91=