Canonical Allele Identifier: CA2272849715
Gene: LINC01483 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854765_69854766delinsCT , CM000679.2:g.69854765_69854766delinsCT GRCh38
NC_000017.10:g.67850906_67850907delinsCT , CM000679.1:g.67850906_67850907delinsCT GRCh37
NC_000017.9:g.65362501_65362502delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109971.1:n.363+9279_363+9280delinsCT
NR_109972.1:n.363+9279_363+9280delinsCT