Canonical Allele Identifier: CA343320498

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192245T>C (hg19) ; chr1:g.161222455T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222455T>C , CM000663.2:g.161222455T>C	GRCh38
NC_000001.10:g.161192245T>C , CM000663.1:g.161192245T>C	GRCh37
NC_000001.9:g.159458869T>C	NCBI36
NG_012043.1:g.6174A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.253A>G MANE Select	ENSP00000356969.3:p.Asn85Asp
ENST00000463273.5:c.253A>G	ENSP00000476740.1:p.Asn85Asp
ENST00000463812.1:c.109A>G	ENSP00000476890.1:p.Asn37Asp
ENST00000464492.5:c.352A>G	ENSP00000476911.1:p.Asn118Asp
ENST00000468465.5:c.109A>G	ENSP00000476662.1:p.Asn37Asp
ENST00000470459.6:c.201-2A>G	ENSP00000477031.1:n.201-2A>G
ENST00000481413.1:n.764A>G
ENST00000481511.5:c.*250A>G	ENSP00000477054.1:n.*250A>G
ENST00000491350.1:c.*36A>G	ENSP00000477353.1:n.*36A>G
NM_001643.1:c.253A>G	NP_001634.1:p.Asn85Asp
NM_001643.2:c.253A>G MANE Select	NP_001634.1:p.Asn85Asp