Canonical Allele Identifier: CA343320486

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192242A>C (hg19) ; chr1:g.161222452A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222452A>C , CM000663.2:g.161222452A>C	GRCh38
NC_000001.10:g.161192242A>C , CM000663.1:g.161192242A>C	GRCh37
NC_000001.9:g.159458866A>C	NCBI36
NG_012043.1:g.6177T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.256T>G MANE Select	ENSP00000356969.3:p.Phe86Val
ENST00000463273.5:c.256T>G	ENSP00000476740.1:p.Phe86Val
ENST00000463812.1:c.112T>G	ENSP00000476890.1:p.Phe38Val
ENST00000464492.5:c.355T>G	ENSP00000476911.1:p.Phe119Val
ENST00000468465.5:c.112T>G	ENSP00000476662.1:p.Phe38Val
ENST00000470459.6:c.202T>G	ENSP00000477031.1:p.Phe68Val
ENST00000481413.1:n.767T>G
ENST00000481511.5:c.*253T>G	ENSP00000477054.1:n.*253T>G
ENST00000491350.1:c.*39T>G	ENSP00000477353.1:n.*39T>G
NM_001643.1:c.256T>G	NP_001634.1:p.Phe86Val
NM_001643.2:c.256T>G MANE Select	NP_001634.1:p.Phe86Val