Canonical Allele Identifier: CA2107004953
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs1593835971

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458051A>G , CM000675.2:g.84458051A>G GRCh38
NC_000013.10:g.85032186A>G , CM000675.1:g.85032186A>G GRCh37
NC_000013.9:g.83930187A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104313A>G
XR_942133.1:n.369-46132T>C
XR_942134.1:n.366-46132T>C