Canonical Allele Identifier: CA254038912
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs1057191405

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458266A>G , CM000675.2:g.84458266A>G GRCh38
NC_000013.10:g.85032401A>G , CM000675.1:g.85032401A>G GRCh37
NC_000013.9:g.83930402A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104098A>G
XR_942133.1:n.369-46347T>C
XR_942134.1:n.366-46347T>C