Canonical Allele Identifier: CA2107004942
Gene: LINC00333 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458041A= , CM000675.2:g.84458041A= GRCh38
NC_000013.10:g.85032176A= , CM000675.1:g.85032176A= GRCh37
NC_000013.9:g.83930177A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046871.1:n.139-104323A=
XR_942133.1:n.369-46122T=
XR_942134.1:n.366-46122T=
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