Canonical Allele Identifier: CA293666663
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs906960218

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854797T>C , CM000679.2:g.69854797T>C GRCh38
NC_000017.10:g.67850938T>C , CM000679.1:g.67850938T>C GRCh37
NC_000017.9:g.65362533T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109971.1:n.363+9311T>C
NR_109972.1:n.363+9311T>C