Canonical Allele Identifier: CA421400054

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192118T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222328T>G , CM000663.2:g.161222328T>G	GRCh38
NC_000001.10:g.161192118T>G , CM000663.1:g.161192118T>G	GRCh37
NC_000001.9:g.159458742T>G	NCBI36
NG_012043.1:g.6301A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.*77A>C MANE Select	ENSP00000356969.3:n.*77A>C
ENST00000463812.1:c.*77A>C	ENSP00000476890.1:n.*77A>C
ENST00000464492.5:c.*77A>C	ENSP00000476911.1:n.*77A>C
ENST00000468465.5:c.*77A>C	ENSP00000476662.1:n.*77A>C
ENST00000470459.6:c.*77A>C	ENSP00000477031.1:n.*77A>C
ENST00000481413.1:n.891A>C
ENST00000481511.5:c.*377A>C	ENSP00000477054.1:n.*377A>C
ENST00000491350.1:c.*163A>C	ENSP00000477353.1:n.*163A>C
NM_001643.1:c.*77A>C	NP_001634.1:n.*77A>C
NM_001643.2:c.*77A>C MANE Select	NP_001634.1:n.*77A>C