Canonical Allele Identifier: CA343320518

Gene: APOA2

Linked Data

• dbSNP Id: rs778751126
• MyVariant Identifiers: chr1:g.161192250A>G (hg19) ; chr1:g.161222460A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222460A>G , CM000663.2:g.161222460A>G	GRCh38
NC_000001.10:g.161192250A>G , CM000663.1:g.161192250A>G	GRCh37
NC_000001.9:g.159458874A>G	NCBI36
NG_012043.1:g.6169T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.248T>C MANE Select	ENSP00000356969.3:p.Leu83Pro
ENST00000463273.5:c.248T>C	ENSP00000476740.1:p.Leu83Pro
ENST00000463812.1:c.104T>C	ENSP00000476890.1:p.Leu35Pro
ENST00000464492.5:c.347T>C	ENSP00000476911.1:p.Leu116Pro
ENST00000468465.5:c.104T>C	ENSP00000476662.1:p.Leu35Pro
ENST00000470459.6:c.201-7T>C	ENSP00000477031.1:n.201-7T>C
ENST00000481413.1:n.759T>C
ENST00000481511.5:c.*245T>C	ENSP00000477054.1:n.*245T>C
ENST00000491350.1:c.*31T>C	ENSP00000477353.1:n.*31T>C
NM_001643.1:c.248T>C	NP_001634.1:p.Leu83Pro
NM_001643.2:c.248T>C MANE Select	NP_001634.1:p.Leu83Pro