Canonical Allele Identifier: CA958336127
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs1879687002

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458328A>T , CM000675.2:g.84458328A>T GRCh38
NC_000013.10:g.85032463A>T , CM000675.1:g.85032463A>T GRCh37
NC_000013.9:g.83930464A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104036A>T
XR_942133.1:n.369-46409T>A
XR_942134.1:n.366-46409T>A