Canonical Allele Identifier: CA2107005030
Gene: LINC00333 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458136G= , CM000675.2:g.84458136G= GRCh38
NC_000013.10:g.85032271G= , CM000675.1:g.85032271G= GRCh37
NC_000013.9:g.83930272G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046871.1:n.139-104228G=
XR_942133.1:n.369-46217C=
XR_942134.1:n.366-46217C=