Canonical Allele Identifier: CA2733995593
Gene: LINC01483 HGNC NCBI

Linked Data

dbSNP Id: rs2143093800

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.69854695A>T , CM000679.2:g.69854695A>T GRCh38
NC_000017.10:g.67850836A>T , CM000679.1:g.67850836A>T GRCh37
NC_000017.9:g.65362431A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109971.1:n.363+9209A>T
NR_109972.1:n.363+9209A>T