Canonical Allele Identifier: CA601827063
Gene: APOA1-AS HGNC NCBI

Linked Data

dbSNP Id: rs1339115094
gnomAD v2: 11-116710677-A-G
gnomAD v3: 11-116839961-A-G
gnomAD v4: 11-116839961-A-G
MyVariant Identifiers: chr11:g.116710677A>G (hg19) chr11:g.116839961A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116839961A>G , CM000673.2:g.116839961A>G GRCh38
NC_000011.9:g.116710677A>G , CM000673.1:g.116710677A>G GRCh37
NC_000011.8:g.116215887A>G NCBI36
NG_012021.1:g.2662T>C , LRG_767:g.2662T>C

Transcript Alleles

HGVS Amino-acid Change
NR_126362.1:n.123+3722A>G
Search 100 bp 5'
Search 100 bp 3'