Canonical Allele Identifier: CA343320429

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192229A>G (hg19) ; chr1:g.161222439A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222439A>G , CM000663.2:g.161222439A>G	GRCh38
NC_000001.10:g.161192229A>G , CM000663.1:g.161192229A>G	GRCh37
NC_000001.9:g.159458853A>G	NCBI36
NG_012043.1:g.6190T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.269T>C MANE Select	ENSP00000356969.3:p.Phe90Ser
ENST00000463273.5:c.269T>C	ENSP00000476740.1:p.Phe90Ser
ENST00000463812.1:c.125T>C	ENSP00000476890.1:p.Phe42Ser
ENST00000464492.5:c.368T>C	ENSP00000476911.1:p.Phe123Ser
ENST00000468465.5:c.125T>C	ENSP00000476662.1:p.Phe42Ser
ENST00000470459.6:c.215T>C	ENSP00000477031.1:p.Phe72Ser
ENST00000481413.1:n.780T>C
ENST00000481511.5:c.*266T>C	ENSP00000477054.1:n.*266T>C
ENST00000491350.1:c.*52T>C	ENSP00000477353.1:n.*52T>C
NM_001643.1:c.269T>C	NP_001634.1:p.Phe90Ser
NM_001643.2:c.269T>C MANE Select	NP_001634.1:p.Phe90Ser