Canonical Allele Identifier: CA1415002851
Gene: LINC01100 HGNC NCBI
IL12A-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1721299752

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.160028128A>G , CM000665.2:g.160028128A>G GRCh38
NC_000003.11:g.159745915A>G , CM000665.1:g.159745915A>G GRCh37
NC_000003.10:g.161228609A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104132.1:n.373+1242A>G (LINC01100)
NR_108088.1:n.518-2594T>C (IL12A-AS1)