Canonical Allele Identifier: CA343320457

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192236T>A (hg19) ; chr1:g.161222446T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222446T>A , CM000663.2:g.161222446T>A	GRCh38
NC_000001.10:g.161192236T>A , CM000663.1:g.161192236T>A	GRCh37
NC_000001.9:g.159458860T>A	NCBI36
NG_012043.1:g.6183A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.262A>T MANE Select	ENSP00000356969.3:p.Ser88Cys
ENST00000463273.5:c.262A>T	ENSP00000476740.1:p.Ser88Cys
ENST00000463812.1:c.118A>T	ENSP00000476890.1:p.Ser40Cys
ENST00000464492.5:c.361A>T	ENSP00000476911.1:p.Ser121Cys
ENST00000468465.5:c.118A>T	ENSP00000476662.1:p.Ser40Cys
ENST00000470459.6:c.208A>T	ENSP00000477031.1:p.Ser70Cys
ENST00000481413.1:n.773A>T
ENST00000481511.5:c.*259A>T	ENSP00000477054.1:n.*259A>T
ENST00000491350.1:c.*45A>T	ENSP00000477353.1:n.*45A>T
NM_001643.1:c.262A>T	NP_001634.1:p.Ser88Cys
NM_001643.2:c.262A>T MANE Select	NP_001634.1:p.Ser88Cys