Canonical Allele Identifier: CA2799969171
Gene: LINC00333 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458049C>A , CM000675.2:g.84458049C>A GRCh38
NC_000013.10:g.85032184C>A , CM000675.1:g.85032184C>A GRCh37
NC_000013.9:g.83930185C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104315C>A
XR_942133.1:n.369-46130G>T
XR_942134.1:n.366-46130G>T