Canonical Allele Identifier: CA421400081

Gene: APOA2

Linked Data

• MyVariant Identifiers: chr1:g.161192122G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222332G>C , CM000663.2:g.161222332G>C	GRCh38
NC_000001.10:g.161192122G>C , CM000663.1:g.161192122G>C	GRCh37
NC_000001.9:g.159458746G>C	NCBI36
NG_012043.1:g.6297C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.*73C>G MANE Select	ENSP00000356969.3:n.*73C>G
ENST00000463812.1:c.*73C>G	ENSP00000476890.1:n.*73C>G
ENST00000464492.5:c.*73C>G	ENSP00000476911.1:n.*73C>G
ENST00000468465.5:c.*73C>G	ENSP00000476662.1:n.*73C>G
ENST00000470459.6:c.*73C>G	ENSP00000477031.1:n.*73C>G
ENST00000481413.1:n.887C>G
ENST00000481511.5:c.*373C>G	ENSP00000477054.1:n.*373C>G
ENST00000491350.1:c.*159C>G	ENSP00000477353.1:n.*159C>G
NM_001643.1:c.*73C>G	NP_001634.1:n.*73C>G
NM_001643.2:c.*73C>G MANE Select	NP_001634.1:n.*73C>G