Canonical Allele Identifier: CA2272849719
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs1917508016

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854782_69854806dup , CM000679.2:g.69854782_69854806dup GRCh38
NC_000017.10:g.67850923_67850947dup , CM000679.1:g.67850923_67850947dup GRCh37
NC_000017.9:g.65362518_65362542dup NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109971.1:n.363+9296_363+9320dup
NR_109972.1:n.363+9296_363+9320dup