Canonical Allele Identifier: CA31634156

Gene: APOA2

Linked Data

• dbSNP Id: rs753545559
• MyVariant Identifiers: chr1:g.161192218C>T (hg19) ; chr1:g.161222428C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222428C>T , CM000663.2:g.161222428C>T	GRCh38
NC_000001.10:g.161192218C>T , CM000663.1:g.161192218C>T	GRCh37
NC_000001.9:g.159458842C>T	NCBI36
NG_012043.1:g.6201G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.280G>A MANE Select	ENSP00000356969.3:p.Gly94Arg
ENST00000463273.5:c.280G>A	ENSP00000476740.1:p.Gly94Arg
ENST00000463812.1:c.136G>A	ENSP00000476890.1:p.Gly46Arg
ENST00000464492.5:c.379G>A	ENSP00000476911.1:p.Gly127Arg
ENST00000468465.5:c.136G>A	ENSP00000476662.1:p.Gly46Arg
ENST00000470459.6:c.226G>A	ENSP00000477031.1:p.Gly76Arg
ENST00000481413.1:n.791G>A
ENST00000481511.5:c.*277G>A	ENSP00000477054.1:n.*277G>A
ENST00000491350.1:c.*63G>A	ENSP00000477353.1:n.*63G>A
NM_001643.1:c.280G>A	NP_001634.1:p.Gly94Arg
NM_001643.2:c.280G>A MANE Select	NP_001634.1:p.Gly94Arg