Canonical Allele Identifier: CA890192634

Gene: APOA2

Linked Data

• dbSNP Id: rs1430117927
• gnomAD v3: 1-161222725-G-T
• gnomAD v4: 1-161222725-G-T
• MyVariant Identifiers: chr1:g.161192515G>T (hg19) ; chr1:g.161222725G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222725G>T , CM000663.2:g.161222725G>T	GRCh38
NC_000001.10:g.161192515G>T , CM000663.1:g.161192515G>T	GRCh37
NC_000001.9:g.159459139G>T	NCBI36
NG_012043.1:g.5904C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.185+193C>A MANE Select	ENSP00000356969.3:n.185+193C>A
ENST00000463273.5:c.185+193C>A	ENSP00000476740.1:n.185+193C>A
ENST00000463812.1:c.41+193C>A	ENSP00000476890.1:n.41+193C>A
ENST00000464492.5:c.284+193C>A	ENSP00000476911.1:n.284+193C>A
ENST00000468465.5:c.41+193C>A	ENSP00000476662.1:n.41+193C>A
ENST00000469730.2:c.185+193C>A	ENSP00000476605.1:n.185+193C>A
ENST00000470459.6:c.185+193C>A	ENSP00000477031.1:n.185+193C>A
ENST00000481413.1:n.696+193C>A
ENST00000481511.5:c.*182+193C>A	ENSP00000477054.1:n.*182+193C>A
ENST00000491350.1:c.53-203C>A	ENSP00000477353.1:n.53-203C>A
NM_001643.1:c.185+193C>A	NP_001634.1:n.185+193C>A
NM_001643.2:c.185+193C>A MANE Select	NP_001634.1:n.185+193C>A