Canonical Allele Identifier: CA2107005110
Gene: LINC00333 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458243T= , CM000675.2:g.84458243T= GRCh38
NC_000013.10:g.85032378T= , CM000675.1:g.85032378T= GRCh37
NC_000013.9:g.83930379T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046871.1:n.139-104121T=
XR_942133.1:n.369-46324A=
XR_942134.1:n.366-46324A=