Canonical Allele Identifier: CA655459778
Gene: LINC00333 HGNC NCBI

Linked Data

COSMIC: COSN20163467
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458294G>A , CM000675.2:g.84458294G>A GRCh38
NC_000013.10:g.85032429G>A , CM000675.1:g.85032429G>A GRCh37
NC_000013.9:g.83930430G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046871.1:n.139-104070G>A
XR_942133.1:n.369-46375C>T
XR_942134.1:n.366-46375C>T
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