Canonical Allele Identifier: CA2107004982
Gene: LINC00333 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458079C= , CM000675.2:g.84458079C= GRCh38
NC_000013.10:g.85032214C= , CM000675.1:g.85032214C= GRCh37
NC_000013.9:g.83930215C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104285C=
XR_942133.1:n.369-46160G=
XR_942134.1:n.366-46160G=