Canonical Allele Identifier: CA601827070
Gene: APOA1-AS HGNC NCBI

Linked Data

dbSNP Id: rs1166623253
gnomAD v2: 11-116710820-A-C
gnomAD v3: 11-116840104-A-C
gnomAD v4: 11-116840104-A-C
MyVariant Identifiers: chr11:g.116710820A>C (hg19) chr11:g.116840104A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116840104A>C , CM000673.2:g.116840104A>C GRCh38
NC_000011.9:g.116710820A>C , CM000673.1:g.116710820A>C GRCh37
NC_000011.8:g.116216030A>C NCBI36
NG_012021.1:g.2519T>G , LRG_767:g.2519T>G

Transcript Alleles

HGVS Amino-acid Change
NR_126362.1:n.123+3865A>C
Search 100 bp 5'
Search 100 bp 3'