Canonical Allele Identifier: CA2272849612
Gene: LINC01483 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854569_69854570delinsAG , CM000679.2:g.69854569_69854570delinsAG GRCh38
NC_000017.10:g.67850710_67850711delinsAG , CM000679.1:g.67850710_67850711delinsAG GRCh37
NC_000017.9:g.65362305_65362306delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109971.1:n.363+9083_363+9084delinsAG
NR_109972.1:n.363+9083_363+9084delinsAG