Canonical Allele Identifier: CA87027164
Gene: LINC01100 HGNC NCBI
IL12A-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs988176794

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.160028124A>T , CM000665.2:g.160028124A>T GRCh38
NC_000003.11:g.159745911A>T , CM000665.1:g.159745911A>T GRCh37
NC_000003.10:g.161228605A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104132.1:n.373+1238A>T (LINC01100)
NR_108088.1:n.518-2590T>A (IL12A-AS1)