Canonical Allele Identifier: CA229327450
Gene: APOA1-AS HGNC NCBI

Linked Data

dbSNP Id: rs528581568
MyVariant Identifiers: chr11:g.116710723C>A (hg19) chr11:g.116840007C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116840007C>A , CM000673.2:g.116840007C>A GRCh38
NC_000011.9:g.116710723C>A , CM000673.1:g.116710723C>A GRCh37
NC_000011.8:g.116215933C>A NCBI36
NG_012021.1:g.2616G>T , LRG_767:g.2616G>T

Transcript Alleles

HGVS Amino-acid Change
NR_126362.1:n.123+3768C>A
Search 100 bp 5'
Search 100 bp 3'