Canonical Allele Identifier: CA2107005051
Gene: LINC00333 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458153A= , CM000675.2:g.84458153A= GRCh38
NC_000013.10:g.85032288A= , CM000675.1:g.85032288A= GRCh37
NC_000013.9:g.83930289A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104211A=
XR_942133.1:n.369-46234T=
XR_942134.1:n.366-46234T=