Canonical Allele Identifier: CA2107005062
Gene: LINC00333 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458172T= , CM000675.2:g.84458172T= GRCh38
NC_000013.10:g.85032307T= , CM000675.1:g.85032307T= GRCh37
NC_000013.9:g.83930308T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104192T=
XR_942133.1:n.369-46253A=
XR_942134.1:n.366-46253A=