Canonical Allele Identifier: CA2810289076
Gene: LINC01483 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854512C>A , CM000679.2:g.69854512C>A GRCh38
NC_000017.10:g.67850653C>A , CM000679.1:g.67850653C>A GRCh37
NC_000017.9:g.65362248C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109971.1:n.363+9026C>A
NR_109972.1:n.363+9026C>A