Canonical Allele Identifier: CA421400085

Gene: APOA2

Linked Data

• dbSNP Id: rs1404201629
• gnomAD v2: 1-161192122-G-A
• gnomAD v4: 1-161222332-G-A
• MyVariant Identifiers: chr1:g.161192122G>A (hg19) ; chr1:g.161222332G>A (hg38)

Genomic Alleles

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

Transcript Alleles

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