Canonical Allele Identifier: CA343320404

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192222T>G (hg19) ; chr1:g.161222432T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222432T>G , CM000663.2:g.161222432T>G	GRCh38
NC_000001.10:g.161192222T>G , CM000663.1:g.161192222T>G	GRCh37
NC_000001.9:g.159458846T>G	NCBI36
NG_012043.1:g.6197A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.276A>C MANE Select	ENSP00000356969.3:p.Glu92Asp
ENST00000463273.5:c.276A>C	ENSP00000476740.1:p.Glu92Asp
ENST00000463812.1:c.132A>C	ENSP00000476890.1:p.Glu44Asp
ENST00000464492.5:c.375A>C	ENSP00000476911.1:p.Glu125Asp
ENST00000468465.5:c.132A>C	ENSP00000476662.1:p.Glu44Asp
ENST00000470459.6:c.222A>C	ENSP00000477031.1:p.Glu74Asp
ENST00000481413.1:n.787A>C
ENST00000481511.5:c.*273A>C	ENSP00000477054.1:n.*273A>C
ENST00000491350.1:c.*59A>C	ENSP00000477353.1:n.*59A>C
NM_001643.1:c.276A>C	NP_001634.1:p.Glu92Asp
NM_001643.2:c.276A>C MANE Select	NP_001634.1:p.Glu92Asp