Canonical Allele Identifier: CA2107004977

Gene: LINC00333

Linked Data

• dbSNP Id: rs1879681598

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.84458069G>T , CM000675.2:g.84458069G>T	GRCh38
NC_000013.10:g.85032204G>T , CM000675.1:g.85032204G>T	GRCh37
NC_000013.9:g.83930205G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046871.1:n.139-104295G>T
XR_942133.1:n.369-46150C>A
XR_942134.1:n.366-46150C>A