Canonical Allele Identifier: CA343320771

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192292T>C (hg19) ; chr1:g.161222502T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222502T>C , CM000663.2:g.161222502T>C	GRCh38
NC_000001.10:g.161192292T>C , CM000663.1:g.161192292T>C	GRCh37
NC_000001.9:g.159458916T>C	NCBI36
NG_012043.1:g.6127A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.206A>G MANE Select	ENSP00000356969.3:p.Lys69Arg
ENST00000463273.5:c.206A>G	ENSP00000476740.1:p.Lys69Arg
ENST00000463812.1:c.62A>G	ENSP00000476890.1:p.Lys21Arg
ENST00000464492.5:c.305A>G	ENSP00000476911.1:p.Lys102Arg
ENST00000468465.5:c.62A>G	ENSP00000476662.1:p.Lys21Arg
ENST00000470459.6:c.200+6A>G	ENSP00000477031.1:n.200+6A>G
ENST00000481413.1:n.717A>G
ENST00000481511.5:c.*203A>G	ENSP00000477054.1:n.*203A>G
ENST00000491350.1:c.73A>G	ENSP00000477353.1:p.Arg25Gly
NM_001643.1:c.206A>G	NP_001634.1:p.Lys69Arg
NM_001643.2:c.206A>G MANE Select	NP_001634.1:p.Lys69Arg