Canonical Allele Identifier: CA2107005081
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs1879684096

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458204C>T , CM000675.2:g.84458204C>T GRCh38
NC_000013.10:g.85032339C>T , CM000675.1:g.85032339C>T GRCh37
NC_000013.9:g.83930340C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046871.1:n.139-104160C>T
XR_942133.1:n.369-46285G>A
XR_942134.1:n.366-46285G>A