Canonical Allele Identifier: CA2648766495

Gene: APOA2

Linked Data

• gnomAD v4: 1-161222539-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222539A>G , CM000663.2:g.161222539A>G	GRCh38
NC_000001.10:g.161192329A>G , CM000663.1:g.161192329A>G	GRCh37
NC_000001.9:g.159458953A>G	NCBI36
NG_012043.1:g.6090T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.186-17T>C MANE Select	ENSP00000356969.3:n.186-17T>C
ENST00000463273.5:c.186-17T>C	ENSP00000476740.1:n.186-17T>C
ENST00000463812.1:c.42-17T>C	ENSP00000476890.1:n.42-17T>C
ENST00000464492.5:c.285-17T>C	ENSP00000476911.1:n.285-17T>C
ENST00000468465.5:c.42-17T>C	ENSP00000476662.1:n.42-17T>C
ENST00000469730.2:c.186-17T>C	ENSP00000476605.1:n.186-17T>C
ENST00000470459.6:c.186-17T>C	ENSP00000477031.1:n.186-17T>C
ENST00000481413.1:n.697-17T>C
ENST00000481511.5:c.*183-17T>C	ENSP00000477054.1:n.*183-17T>C
ENST00000491350.1:c.53-17T>C	ENSP00000477353.1:n.53-17T>C
NM_001643.1:c.186-17T>C	NP_001634.1:n.186-17T>C
NM_001643.2:c.186-17T>C MANE Select	NP_001634.1:n.186-17T>C