Canonical Allele Identifier: CA343320441

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192232T>G (hg19) ; chr1:g.161222442T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222442T>G , CM000663.2:g.161222442T>G	GRCh38
NC_000001.10:g.161192232T>G , CM000663.1:g.161192232T>G	GRCh37
NC_000001.9:g.159458856T>G	NCBI36
NG_012043.1:g.6187A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.266A>C MANE Select	ENSP00000356969.3:p.Tyr89Ser
ENST00000463273.5:c.266A>C	ENSP00000476740.1:p.Tyr89Ser
ENST00000463812.1:c.122A>C	ENSP00000476890.1:p.Tyr41Ser
ENST00000464492.5:c.365A>C	ENSP00000476911.1:p.Tyr122Ser
ENST00000468465.5:c.122A>C	ENSP00000476662.1:p.Tyr41Ser
ENST00000470459.6:c.212A>C	ENSP00000477031.1:p.Tyr71Ser
ENST00000481413.1:n.777A>C
ENST00000481511.5:c.*263A>C	ENSP00000477054.1:n.*263A>C
ENST00000491350.1:c.*49A>C	ENSP00000477353.1:n.*49A>C
NM_001643.1:c.266A>C	NP_001634.1:p.Tyr89Ser
NM_001643.2:c.266A>C MANE Select	NP_001634.1:p.Tyr89Ser