Canonical Allele Identifier: CA229327680
Gene: APOA1-AS HGNC NCBI

Linked Data

dbSNP Id: rs181696828
gnomAD v2: 11-116711063-C-T
gnomAD v3: 11-116840347-C-T
gnomAD v4: 11-116840347-C-T
MyVariant Identifiers: chr11:g.116711063C>T (hg19) chr11:g.116840347C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116840347C>T , CM000673.2:g.116840347C>T GRCh38
NC_000011.9:g.116711063C>T , CM000673.1:g.116711063C>T GRCh37
NC_000011.8:g.116216273C>T NCBI36
NG_012021.1:g.2276G>A , LRG_767:g.2276G>A

Transcript Alleles

HGVS Amino-acid change
NR_126362.1:n.123+4108C>T
Search 100 bp 5'
Search 100 bp 3'