Canonical Allele Identifier: CA774555004
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs1263771632

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854664C>T , CM000679.2:g.69854664C>T GRCh38
NC_000017.10:g.67850805C>T , CM000679.1:g.67850805C>T GRCh37
NC_000017.9:g.65362400C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_109971.1:n.363+9178C>T
NR_109972.1:n.363+9178C>T