Canonical Allele Identifier: CA343320308

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192195T>C (hg19) ; chr1:g.161222405T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222405T>C , CM000663.2:g.161222405T>C	GRCh38
NC_000001.10:g.161192195T>C , CM000663.1:g.161192195T>C	GRCh37
NC_000001.9:g.159458819T>C	NCBI36
NG_012043.1:g.6224A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.303A>G MANE Select	ENSP00000356969.3:p.Ter101Trp
ENST00000463812.1:c.159A>G	ENSP00000476890.1:p.Ter53Trp
ENST00000464492.5:c.402A>G	ENSP00000476911.1:p.Ter134Trp
ENST00000468465.5:c.159A>G	ENSP00000476662.1:p.Ter53Trp
ENST00000470459.6:c.249A>G	ENSP00000477031.1:p.Ter83Trp
ENST00000481413.1:n.814A>G
ENST00000481511.5:c.*300A>G	ENSP00000477054.1:n.*300A>G
ENST00000491350.1:c.*86A>G	ENSP00000477353.1:n.*86A>G
NM_001643.1:c.303A>G	NP_001634.1:p.Ter101Trp
NM_001643.2:c.303A>G MANE Select	NP_001634.1:p.Ter101Trp