Canonical Allele Identifier: CA672207734
Gene: APOA1-AS HGNC NCBI

Linked Data

dbSNP Id: rs1006350864
gnomAD v3: 11-116840062-G-T
gnomAD v4: 11-116840062-G-T
MyVariant Identifiers: chr11:g.116710778G>T (hg19) chr11:g.116840062G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116840062G>T , CM000673.2:g.116840062G>T GRCh38
NC_000011.9:g.116710778G>T , CM000673.1:g.116710778G>T GRCh37
NC_000011.8:g.116215988G>T NCBI36
NG_012021.1:g.2561C>A , LRG_767:g.2561C>A

Transcript Alleles

HGVS Amino-acid Change
NR_126362.1:n.123+3823G>T
Search 100 bp 5'
Search 100 bp 3'