Canonical Allele Identifier: CA293666660
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs2366017

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854760G>A , CM000679.2:g.69854760G>A GRCh38
NC_000017.10:g.67850901G>A , CM000679.1:g.67850901G>A GRCh37
NC_000017.9:g.65362496G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109971.1:n.363+9274G>A
NR_109972.1:n.363+9274G>A