Canonical Allele Identifier: CA958336066
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs1879684264

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458210_84458219dup , CM000675.2:g.84458210_84458219dup GRCh38
NC_000013.10:g.85032345_85032354dup , CM000675.1:g.85032345_85032354dup GRCh37
NC_000013.9:g.83930346_83930355dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104154_139-104145dup
XR_942133.1:n.369-46300_369-46291dup
XR_942134.1:n.366-46300_366-46291dup