Canonical Allele Identifier: CA774555006
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs1341133127

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854674_69854677del , CM000679.2:g.69854674_69854677del GRCh38
NC_000017.10:g.67850815_67850818del , CM000679.1:g.67850815_67850818del GRCh37
NC_000017.9:g.65362410_65362413del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109971.1:n.363+9188_363+9191del
NR_109972.1:n.363+9188_363+9191del