Canonical Allele Identifier: CA2107005045
Gene: LINC00333 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458149C= , CM000675.2:g.84458149C= GRCh38
NC_000013.10:g.85032284C= , CM000675.1:g.85032284C= GRCh37
NC_000013.9:g.83930285C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046871.1:n.139-104215C=
XR_942133.1:n.369-46230G=
XR_942134.1:n.366-46230G=