Canonical Allele Identifier: CA421400114
Gene: APOA2 HGNC NCBI

Linked Data

gnomAD v4: 1-161222335-A-G
MyVariant Identifiers: chr1:g.161192125A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161222335A>G , CM000663.2:g.161222335A>G GRCh38
NC_000001.10:g.161192125A>G , CM000663.1:g.161192125A>G GRCh37
NC_000001.9:g.159458749A>G NCBI36
NG_012043.1:g.6294T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367990.7:c.*70T>C MANE Select ENSP00000356969.3:n.*70T>C
ENST00000463812.1:c.*70T>C ENSP00000476890.1:n.*70T>C
ENST00000464492.5:c.*70T>C ENSP00000476911.1:n.*70T>C
ENST00000468465.5:c.*70T>C ENSP00000476662.1:n.*70T>C
ENST00000470459.6:c.*70T>C ENSP00000477031.1:n.*70T>C
ENST00000481413.1:n.884T>C
ENST00000481511.5:c.*370T>C ENSP00000477054.1:n.*370T>C
ENST00000491350.1:c.*156T>C ENSP00000477353.1:n.*156T>C
NM_001643.1:c.*70T>C NP_001634.1:n.*70T>C
NM_001643.2:c.*70T>C MANE Select NP_001634.1:n.*70T>C
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