Canonical Allele Identifier: CA672207774
Gene: APOA1-AS HGNC NCBI

Linked Data

dbSNP Id: rs1371729095
gnomAD v3: 11-116840170-A-G
gnomAD v4: 11-116840170-A-G
MyVariant Identifiers: chr11:g.116710886A>G (hg19) chr11:g.116840170A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116840170A>G , CM000673.2:g.116840170A>G GRCh38
NC_000011.9:g.116710886A>G , CM000673.1:g.116710886A>G GRCh37
NC_000011.8:g.116216096A>G NCBI36
NG_012021.1:g.2453T>C , LRG_767:g.2453T>C

Transcript Alleles

HGVS Amino-acid Change
NR_126362.1:n.123+3931A>G
Search 100 bp 5'
Search 100 bp 3'