Canonical Allele Identifier: CA2107005032
Gene: LINC00333 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458137G= , CM000675.2:g.84458137G= GRCh38
NC_000013.10:g.85032272G= , CM000675.1:g.85032272G= GRCh37
NC_000013.9:g.83930273G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046871.1:n.139-104227G=
XR_942133.1:n.369-46218C=
XR_942134.1:n.366-46218C=