Canonical Allele Identifier: CA2272849669
Gene: LINC01483 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854671_69854675delinsTGAAA , CM000679.2:g.69854671_69854675delinsTGAAA GRCh38
NC_000017.10:g.67850812_67850816delinsTGAAA , CM000679.1:g.67850812_67850816delinsTGAAA GRCh37
NC_000017.9:g.65362407_65362411delinsTGAAA NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109971.1:n.363+9185_363+9189delinsTGAAA
NR_109972.1:n.363+9185_363+9189delinsTGAAA