Canonical Allele Identifier: CA601827062
Gene: APOA1-AS HGNC NCBI

Linked Data

dbSNP Id: rs1295339818
gnomAD v2: 11-116710665-G-A
gnomAD v3: 11-116839949-G-A
gnomAD v4: 11-116839949-G-A
MyVariant Identifiers: chr11:g.116710665G>A (hg19) chr11:g.116839949G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116839949G>A , CM000673.2:g.116839949G>A GRCh38
NC_000011.9:g.116710665G>A , CM000673.1:g.116710665G>A GRCh37
NC_000011.8:g.116215875G>A NCBI36
NG_012021.1:g.2674C>T , LRG_767:g.2674C>T

Transcript Alleles

HGVS Amino-acid Change
NR_126362.1:n.123+3710G>A
Search 100 bp 5'
Search 100 bp 3'