Canonical Allele Identifier: CA2107005160

Gene: LINC00333

Linked Data

• dbSNP Id: rs917239209

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.84458286A>T , CM000675.2:g.84458286A>T	GRCh38
NC_000013.10:g.85032421A>T , CM000675.1:g.85032421A>T	GRCh37
NC_000013.9:g.83930422A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046871.1:n.139-104078A>T
XR_942133.1:n.369-46367T>A
XR_942134.1:n.366-46367T>A