Canonical Allele Identifier: CA672207792

Gene: APOA1-AS

Linked Data

• dbSNP Id: rs1455073773
• gnomAD v3: 11-116840207-G-A
• gnomAD v4: 11-116840207-G-A
• MyVariant Identifiers: chr11:g.116710923G>A (hg19) ; chr11:g.116840207G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116840207G>A , CM000673.2:g.116840207G>A	GRCh38
NC_000011.9:g.116710923G>A , CM000673.1:g.116710923G>A	GRCh37
NC_000011.8:g.116216133G>A	NCBI36
NG_012021.1:g.2416C>T , LRG_767:g.2416C>T

Transcript Alleles

HGVS	Amino-acid Change
NR_126362.1:n.123+3968G>A