Canonical Allele Identifier: CA1209076

Gene: APOA2

Linked Data

• dbSNP Id: rs749315211
• ExAC: 1:161192139 T / C
• gnomAD v2: 1-161192139-T-C
• gnomAD v3: 1-161222349-T-C
• gnomAD v4: 1-161222349-T-C
• MyVariant Identifiers: chr1:g.161192139T>C (hg19) ; chr1:g.161222349T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161222349T>C , CM000663.2:g.161222349T>C	GRCh38
NC_000001.10:g.161192139T>C , CM000663.1:g.161192139T>C	GRCh37
NC_000001.9:g.159458763T>C	NCBI36
NG_012043.1:g.6280A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367990.7:c.*56A>G MANE Select	ENSP00000356969.3:n.*56A>G
ENST00000463812.1:c.*56A>G	ENSP00000476890.1:n.*56A>G
ENST00000464492.5:c.*56A>G	ENSP00000476911.1:n.*56A>G
ENST00000468465.5:c.*56A>G	ENSP00000476662.1:n.*56A>G
ENST00000470459.6:c.*56A>G	ENSP00000477031.1:n.*56A>G
ENST00000481413.1:n.870A>G
ENST00000481511.5:c.*356A>G	ENSP00000477054.1:n.*356A>G
ENST00000491350.1:c.*142A>G	ENSP00000477353.1:n.*142A>G
NM_001643.1:c.*56A>G	NP_001634.1:n.*56A>G
NM_001643.2:c.*56A>G MANE Select	NP_001634.1:n.*56A>G