Canonical Allele Identifier: CA229327408
Gene: APOA1-AS HGNC NCBI

Linked Data

dbSNP Id: rs145636406
gnomAD v3: 11-116839974-T-C
gnomAD v4: 11-116839974-T-C
MyVariant Identifiers: chr11:g.116710690T>C (hg19) chr11:g.116839974T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116839974T>C , CM000673.2:g.116839974T>C GRCh38
NC_000011.9:g.116710690T>C , CM000673.1:g.116710690T>C GRCh37
NC_000011.8:g.116215900T>C NCBI36
NG_012021.1:g.2649A>G , LRG_767:g.2649A>G

Transcript Alleles

HGVS Amino-acid Change
NR_126362.1:n.123+3735T>C
Search 100 bp 5'
Search 100 bp 3'