Canonical Allele Identifier: CA2272849698
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs1917507416

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854744dup , CM000679.2:g.69854744dup GRCh38
NC_000017.10:g.67850885dup , CM000679.1:g.67850885dup GRCh37
NC_000017.9:g.65362480dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109971.1:n.363+9258dup
NR_109972.1:n.363+9258dup