Canonical Allele Identifier: CA2107085312
Gene: LINC00333 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84603661T= , CM000675.2:g.84603661T= GRCh38
NC_000013.10:g.85177796T= , CM000675.1:g.85177796T= GRCh37
NC_000013.9:g.84075797T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046871.1:n.750-3045T=
XR_942132.1:n.103-2012A=