Canonical Allele Identifier: CA343320435

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192230A>C (hg19) ; chr1:g.161222440A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222440A>C , CM000663.2:g.161222440A>C	GRCh38
NC_000001.10:g.161192230A>C , CM000663.1:g.161192230A>C	GRCh37
NC_000001.9:g.159458854A>C	NCBI36
NG_012043.1:g.6189T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.268T>G MANE Select	ENSP00000356969.3:p.Phe90Val
ENST00000463273.5:c.268T>G	ENSP00000476740.1:p.Phe90Val
ENST00000463812.1:c.124T>G	ENSP00000476890.1:p.Phe42Val
ENST00000464492.5:c.367T>G	ENSP00000476911.1:p.Phe123Val
ENST00000468465.5:c.124T>G	ENSP00000476662.1:p.Phe42Val
ENST00000470459.6:c.214T>G	ENSP00000477031.1:p.Phe72Val
ENST00000481413.1:n.779T>G
ENST00000481511.5:c.*265T>G	ENSP00000477054.1:n.*265T>G
ENST00000491350.1:c.*51T>G	ENSP00000477353.1:n.*51T>G
NM_001643.1:c.268T>G	NP_001634.1:p.Phe90Val
NM_001643.2:c.268T>G MANE Select	NP_001634.1:p.Phe90Val