Canonical Allele Identifier: CA672207775

Gene: APOA1-AS

Linked Data

• dbSNP Id: rs1327659546
• gnomAD v3: 11-116840174-T-C
• gnomAD v4: 11-116840174-T-C
• MyVariant Identifiers: chr11:g.116710890T>C (hg19) ; chr11:g.116840174T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116840174T>C , CM000673.2:g.116840174T>C	GRCh38
NC_000011.9:g.116710890T>C , CM000673.1:g.116710890T>C	GRCh37
NC_000011.8:g.116216100T>C	NCBI36
NG_012021.1:g.2449A>G , LRG_767:g.2449A>G

Transcript Alleles

HGVS	Amino-acid Change
NR_126362.1:n.123+3935T>C