Canonical Allele Identifier: CA476869446

Gene: APOA1-AS

Linked Data

• dbSNP Id: rs1237626140
• gnomAD v3: 11-116840333-C-T
• gnomAD v4: 11-116840333-C-T
• MyVariant Identifiers: chr11:g.116711049C>T (hg19) ; chr11:g.116840333C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116840333C>T , CM000673.2:g.116840333C>T	GRCh38
NC_000011.9:g.116711049C>T , CM000673.1:g.116711049C>T	GRCh37
NC_000011.8:g.116216259C>T	NCBI36
NG_012021.1:g.2290G>A , LRG_767:g.2290G>A

Transcript Alleles

HGVS	Amino-acid Change
NR_126362.1:n.123+4094C>T