Canonical Allele Identifier: CA2107005132
Gene: LINC00333 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458266A= , CM000675.2:g.84458266A= GRCh38
NC_000013.10:g.85032401A= , CM000675.1:g.85032401A= GRCh37
NC_000013.9:g.83930402A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104098A=
XR_942133.1:n.369-46347T=
XR_942134.1:n.366-46347T=