Canonical Allele Identifier: CA672207703
Gene: APOA1-AS HGNC NCBI

Linked Data

dbSNP Id: rs1161183643
gnomAD v3: 11-116840004-G-A
gnomAD v4: 11-116840004-G-A
MyVariant Identifiers: chr11:g.116710720G>A (hg19) chr11:g.116840004G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116840004G>A , CM000673.2:g.116840004G>A GRCh38
NC_000011.9:g.116710720G>A , CM000673.1:g.116710720G>A GRCh37
NC_000011.8:g.116215930G>A NCBI36
NG_012021.1:g.2619C>T , LRG_767:g.2619C>T

Transcript Alleles

HGVS Amino-acid Change
NR_126362.1:n.123+3765G>A
Search 100 bp 5'
Search 100 bp 3'