Canonical Allele Identifier: CA229327388
Gene: APOA1-AS HGNC NCBI

Linked Data

dbSNP Id: rs972368600
gnomAD v3: 11-116839933-T-C
gnomAD v4: 11-116839933-T-C
MyVariant Identifiers: chr11:g.116710649T>C (hg19) chr11:g.116839933T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116839933T>C , CM000673.2:g.116839933T>C GRCh38
NC_000011.9:g.116710649T>C , CM000673.1:g.116710649T>C GRCh37
NC_000011.8:g.116215859T>C NCBI36
NG_012021.1:g.2690A>G , LRG_767:g.2690A>G

Transcript Alleles

HGVS Amino-acid Change
NR_126362.1:n.123+3694T>C
Search 100 bp 5'
Search 100 bp 3'