Canonical Allele Identifier: CA2107004929
Gene: LINC00333 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458020T= , CM000675.2:g.84458020T= GRCh38
NC_000013.10:g.85032155T= , CM000675.1:g.85032155T= GRCh37
NC_000013.9:g.83930156T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104344T=
XR_942133.1:n.369-46101A=
XR_942134.1:n.366-46101A=
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