Canonical Allele Identifier: CA31634343

Gene: APOA2

Linked Data

• dbSNP Id: rs935199577
• gnomAD v3: 1-161222646-C-A
• gnomAD v4: 1-161222646-C-A
• MyVariant Identifiers: chr1:g.161192436C>A (hg19) ; chr1:g.161222646C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222646C>A , CM000663.2:g.161222646C>A	GRCh38
NC_000001.10:g.161192436C>A , CM000663.1:g.161192436C>A	GRCh37
NC_000001.9:g.159459060C>A	NCBI36
NG_012043.1:g.5983G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.186-124G>T MANE Select	ENSP00000356969.3:n.186-124G>T
ENST00000463273.5:c.186-124G>T	ENSP00000476740.1:n.186-124G>T
ENST00000463812.1:c.42-124G>T	ENSP00000476890.1:n.42-124G>T
ENST00000464492.5:c.285-124G>T	ENSP00000476911.1:n.285-124G>T
ENST00000468465.5:c.42-124G>T	ENSP00000476662.1:n.42-124G>T
ENST00000469730.2:c.186-124G>T	ENSP00000476605.1:n.186-124G>T
ENST00000470459.6:c.186-124G>T	ENSP00000477031.1:n.186-124G>T
ENST00000481413.1:n.697-124G>T
ENST00000481511.5:c.*183-124G>T	ENSP00000477054.1:n.*183-124G>T
ENST00000491350.1:c.53-124G>T	ENSP00000477353.1:n.53-124G>T
NM_001643.1:c.186-124G>T	NP_001634.1:n.186-124G>T
NM_001643.2:c.186-124G>T MANE Select	NP_001634.1:n.186-124G>T