Canonical Allele Identifier: CA958335970
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs1879681046

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458044G>T , CM000675.2:g.84458044G>T GRCh38
NC_000013.10:g.85032179G>T , CM000675.1:g.85032179G>T GRCh37
NC_000013.9:g.83930180G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104320G>T
XR_942133.1:n.369-46125C>A
XR_942134.1:n.366-46125C>A