Canonical Allele Identifier: CA87027161
Gene: LINC01100 HGNC NCBI
IL12A-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs545522034

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.160028092A>C , CM000665.2:g.160028092A>C GRCh38
NC_000003.11:g.159745879A>C , CM000665.1:g.159745879A>C GRCh37
NC_000003.10:g.161228573A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104132.1:n.373+1206A>C (LINC01100)
NR_108088.1:n.518-2558T>G (IL12A-AS1)