Canonical Allele Identifier: CA1209092

Gene: APOA2

Linked Data

• dbSNP Id: rs777908160
• ExAC: 1:161192241 A / G
• MyVariant Identifiers: chr1:g.161192241A>G (hg19) ; chr1:g.161222451A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222451A>G , CM000663.2:g.161222451A>G	GRCh38
NC_000001.10:g.161192241A>G , CM000663.1:g.161192241A>G	GRCh37
NC_000001.9:g.159458865A>G	NCBI36
NG_012043.1:g.6178T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.257T>C MANE Select	ENSP00000356969.3:p.Phe86Ser
ENST00000463273.5:c.257T>C	ENSP00000476740.1:p.Phe86Ser
ENST00000463812.1:c.113T>C	ENSP00000476890.1:p.Phe38Ser
ENST00000464492.5:c.356T>C	ENSP00000476911.1:p.Phe119Ser
ENST00000468465.5:c.113T>C	ENSP00000476662.1:p.Phe38Ser
ENST00000470459.6:c.203T>C	ENSP00000477031.1:p.Phe68Ser
ENST00000481413.1:n.768T>C
ENST00000481511.5:c.*254T>C	ENSP00000477054.1:n.*254T>C
ENST00000491350.1:c.*40T>C	ENSP00000477353.1:n.*40T>C
NM_001643.1:c.257T>C	NP_001634.1:p.Phe86Ser
NM_001643.2:c.257T>C MANE Select	NP_001634.1:p.Phe86Ser