Canonical Allele Identifier: CA229327395
Gene: APOA1-AS HGNC NCBI

Linked Data

dbSNP Id: rs955107721
MyVariant Identifiers: chr11:g.116710662T>G (hg19) chr11:g.116839946T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116839946T>G , CM000673.2:g.116839946T>G GRCh38
NC_000011.9:g.116710662T>G , CM000673.1:g.116710662T>G GRCh37
NC_000011.8:g.116215872T>G NCBI36
NG_012021.1:g.2677A>C , LRG_767:g.2677A>C

Transcript Alleles

HGVS Amino-acid Change
NR_126362.1:n.123+3707T>G
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