Canonical Allele Identifier: CA343320504

Gene: APOA2

Linked Data

• gnomAD v4: 1-161222457-A-G
• MyVariant Identifiers: chr1:g.161192247A>G (hg19) ; chr1:g.161222457A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222457A>G , CM000663.2:g.161222457A>G	GRCh38
NC_000001.10:g.161192247A>G , CM000663.1:g.161192247A>G	GRCh37
NC_000001.9:g.159458871A>G	NCBI36
NG_012043.1:g.6172T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367990.7:c.251T>C MANE Select	ENSP00000356969.3:p.Val84Ala
ENST00000463273.5:c.251T>C	ENSP00000476740.1:p.Val84Ala
ENST00000463812.1:c.107T>C	ENSP00000476890.1:p.Val36Ala
ENST00000464492.5:c.350T>C	ENSP00000476911.1:p.Val117Ala
ENST00000468465.5:c.107T>C	ENSP00000476662.1:p.Val36Ala
ENST00000470459.6:c.201-4T>C	ENSP00000477031.1:n.201-4T>C
ENST00000481413.1:n.762T>C
ENST00000481511.5:c.*248T>C	ENSP00000477054.1:n.*248T>C
ENST00000491350.1:c.*34T>C	ENSP00000477353.1:n.*34T>C
NM_001643.1:c.251T>C	NP_001634.1:p.Val84Ala
NM_001643.2:c.251T>C MANE Select	NP_001634.1:p.Val84Ala