Canonical Allele Identifier: CA2107005230
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs899346865

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458345G>A , CM000675.2:g.84458345G>A GRCh38
NC_000013.10:g.85032480G>A , CM000675.1:g.85032480G>A GRCh37
NC_000013.9:g.83930481G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104019G>A
XR_942133.1:n.369-46426C>T
XR_942134.1:n.366-46426C>T