Canonical Allele Identifier: CA2107005141
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs1879685609
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458276G>C , CM000675.2:g.84458276G>C GRCh38
NC_000013.10:g.85032411G>C , CM000675.1:g.85032411G>C GRCh37
NC_000013.9:g.83930412G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046871.1:n.139-104088G>C
XR_942133.1:n.369-46357C>G
XR_942134.1:n.366-46357C>G
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