Canonical Allele Identifier: CA343320773

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192293T>A (hg19) ; chr1:g.161222503T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222503T>A , CM000663.2:g.161222503T>A	GRCh38
NC_000001.10:g.161192293T>A , CM000663.1:g.161192293T>A	GRCh37
NC_000001.9:g.159458917T>A	NCBI36
NG_012043.1:g.6126A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.205A>T MANE Select	ENSP00000356969.3:p.Lys69Ter
ENST00000463273.5:c.205A>T	ENSP00000476740.1:p.Lys69Ter
ENST00000463812.1:c.61A>T	ENSP00000476890.1:p.Lys21Ter
ENST00000464492.5:c.304A>T	ENSP00000476911.1:p.Lys102Ter
ENST00000468465.5:c.61A>T	ENSP00000476662.1:p.Lys21Ter
ENST00000470459.6:c.200+5A>T	ENSP00000477031.1:n.200+5A>T
ENST00000481413.1:n.716A>T
ENST00000481511.5:c.*202A>T	ENSP00000477054.1:n.*202A>T
ENST00000491350.1:c.72A>T	ENSP00000477353.1:p.Gln24His
NM_001643.1:c.205A>T	NP_001634.1:p.Lys69Ter
NM_001643.2:c.205A>T MANE Select	NP_001634.1:p.Lys69Ter