Canonical Allele Identifier: CA229327420
Gene: APOA1-AS HGNC NCBI

Linked Data

dbSNP Id: rs913146729
gnomAD v3: 11-116839979-A-T
gnomAD v4: 11-116839979-A-T
MyVariant Identifiers: chr11:g.116710695A>T (hg19) chr11:g.116839979A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116839979A>T , CM000673.2:g.116839979A>T GRCh38
NC_000011.9:g.116710695A>T , CM000673.1:g.116710695A>T GRCh37
NC_000011.8:g.116215905A>T NCBI36
NG_012021.1:g.2644T>A , LRG_767:g.2644T>A

Transcript Alleles

HGVS Amino-acid Change
NR_126362.1:n.123+3740A>T
Search 100 bp 5'
Search 100 bp 3'