Canonical Allele Identifier: CA2107005162
Gene: LINC00333 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458286A= , CM000675.2:g.84458286A= GRCh38
NC_000013.10:g.85032421A= , CM000675.1:g.85032421A= GRCh37
NC_000013.9:g.83930422A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104078A=
XR_942133.1:n.369-46367T=
XR_942134.1:n.366-46367T=
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