Canonical Allele Identifier: CA2107004944
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs1721272573

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458042G>C , CM000675.2:g.84458042G>C GRCh38
NC_000013.10:g.85032177G>C , CM000675.1:g.85032177G>C GRCh37
NC_000013.9:g.83930178G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104322G>C
XR_942133.1:n.369-46123C>G
XR_942134.1:n.366-46123C>G