Canonical Allele Identifier: CA421401520

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192273C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222483C>G , CM000663.2:g.161222483C>G	GRCh38
NC_000001.10:g.161192273C>G , CM000663.1:g.161192273C>G	GRCh37
NC_000001.9:g.159458897C>G	NCBI36
NG_012043.1:g.6146G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.225G>C MANE Select	ENSP00000356969.3:p.Leu75=
ENST00000463273.5:c.225G>C	ENSP00000476740.1:p.Leu75=
ENST00000463812.1:c.81G>C	ENSP00000476890.1:p.Leu27=
ENST00000464492.5:c.324G>C	ENSP00000476911.1:p.Leu108=
ENST00000468465.5:c.81G>C	ENSP00000476662.1:p.Leu27=
ENST00000470459.6:c.200+25G>C	ENSP00000477031.1:n.200+25G>C
ENST00000481413.1:n.736G>C
ENST00000481511.5:c.*222G>C	ENSP00000477054.1:n.*222G>C
ENST00000491350.1:c.*8G>C	ENSP00000477353.1:n.*8G>C
NM_001643.1:c.225G>C	NP_001634.1:p.Leu75=
NM_001643.2:c.225G>C MANE Select	NP_001634.1:p.Leu75=