Canonical Allele Identifier: CA672207708
Gene: APOA1-AS HGNC NCBI

Linked Data

dbSNP Id: rs1216679902
MyVariant Identifiers: chr11:g.116710744G>C (hg19) chr11:g.116840028G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116840028G>C , CM000673.2:g.116840028G>C GRCh38
NC_000011.9:g.116710744G>C , CM000673.1:g.116710744G>C GRCh37
NC_000011.8:g.116215954G>C NCBI36
NG_012021.1:g.2595C>G , LRG_767:g.2595C>G

Transcript Alleles

HGVS Amino-acid Change
NR_126362.1:n.123+3789G>C
Search 100 bp 5'
Search 100 bp 3'