Canonical Allele Identifier: CA672207730
Gene: APOA1-AS HGNC NCBI

Linked Data

dbSNP Id: rs937341954
gnomAD v3: 11-116840048-C-G
gnomAD v4: 11-116840048-C-G
MyVariant Identifiers: chr11:g.116710764C>G (hg19) chr11:g.116840048C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116840048C>G , CM000673.2:g.116840048C>G GRCh38
NC_000011.9:g.116710764C>G , CM000673.1:g.116710764C>G GRCh37
NC_000011.8:g.116215974C>G NCBI36
NG_012021.1:g.2575G>C , LRG_767:g.2575G>C

Transcript Alleles

HGVS Amino-acid Change
NR_126362.1:n.123+3809C>G
Search 100 bp 5'
Search 100 bp 3'