Canonical Allele Identifier: CA958349986
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs993416138

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84603659A>T , CM000675.2:g.84603659A>T GRCh38
NC_000013.10:g.85177794A>T , CM000675.1:g.85177794A>T GRCh37
NC_000013.9:g.84075795A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046871.1:n.750-3047A>T
XR_942132.1:n.103-2010T>A