Canonical Allele Identifier: CA293666661
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs1046401396

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854765C>T , CM000679.2:g.69854765C>T GRCh38
NC_000017.10:g.67850906C>T , CM000679.1:g.67850906C>T GRCh37
NC_000017.9:g.65362501C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109971.1:n.363+9279C>T
NR_109972.1:n.363+9279C>T