Canonical Allele Identifier: CA2107005067
Gene: LINC00333 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458176C= , CM000675.2:g.84458176C= GRCh38
NC_000013.10:g.85032311C= , CM000675.1:g.85032311C= GRCh37
NC_000013.9:g.83930312C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046871.1:n.139-104188C=
XR_942133.1:n.369-46257G=
XR_942134.1:n.366-46257G=
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