Canonical Allele Identifier: CA421400049
Gene: APOA2 HGNC NCBI

Linked Data

gnomAD v4: 1-161222327-G-T
MyVariant Identifiers: chr1:g.161192117G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161222327G>T , CM000663.2:g.161222327G>T GRCh38
NC_000001.10:g.161192117G>T , CM000663.1:g.161192117G>T GRCh37
NC_000001.9:g.159458741G>T NCBI36
NG_012043.1:g.6302C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367990.7:c.*78C>A MANE Select ENSP00000356969.3:n.*78C>A
ENST00000463812.1:c.*78C>A ENSP00000476890.1:n.*78C>A
ENST00000464492.5:c.*78C>A ENSP00000476911.1:n.*78C>A
ENST00000468465.5:c.*78C>A ENSP00000476662.1:n.*78C>A
ENST00000470459.6:c.*78C>A ENSP00000477031.1:n.*78C>A
ENST00000481413.1:n.892C>A
ENST00000481511.5:c.*378C>A ENSP00000477054.1:n.*378C>A
ENST00000491350.1:c.*164C>A ENSP00000477353.1:n.*164C>A
NM_001643.1:c.*78C>A NP_001634.1:n.*78C>A
NM_001643.2:c.*78C>A MANE Select NP_001634.1:n.*78C>A
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