Canonical Allele Identifier: CA2107004968
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs1879681390

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458063_84458064del , CM000675.2:g.84458063_84458064del GRCh38
NC_000013.10:g.85032198_85032199del , CM000675.1:g.85032198_85032199del GRCh37
NC_000013.9:g.83930199_83930200del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046871.1:n.139-104301_139-104300del
XR_942133.1:n.369-46144_369-46143del
XR_942134.1:n.366-46144_366-46143del