Canonical Allele Identifier: CA229327470
Gene: APOA1-AS HGNC NCBI

Linked Data

dbSNP Id: rs937341954
MyVariant Identifiers: chr11:g.116840048C>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116840048C>A , CM000673.2:g.116840048C>A GRCh38
NC_000011.9:g.116710764C>A , CM000673.1:g.116710764C>A GRCh37
NC_000011.8:g.116215974C>A NCBI36
NG_012021.1:g.2575G>T , LRG_767:g.2575G>T

Transcript Alleles

HGVS Amino-acid Change
NR_126362.1:n.123+3809C>A