Canonical Allele Identifier: CA229327400
Gene: APOA1-AS HGNC NCBI

Linked Data

dbSNP Id: rs1047164591
gnomAD v3: 11-116839973-G-C
gnomAD v4: 11-116839973-G-C
MyVariant Identifiers: chr11:g.116710689G>C (hg19) chr11:g.116839973G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116839973G>C , CM000673.2:g.116839973G>C GRCh38
NC_000011.9:g.116710689G>C , CM000673.1:g.116710689G>C GRCh37
NC_000011.8:g.116215899G>C NCBI36
NG_012021.1:g.2650C>G , LRG_767:g.2650C>G

Transcript Alleles

HGVS Amino-acid Change
NR_126362.1:n.123+3734G>C
Search 100 bp 5'
Search 100 bp 3'