Canonical Allele Identifier: CA2107004991
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs1879682002

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458087T>C , CM000675.2:g.84458087T>C GRCh38
NC_000013.10:g.85032222T>C , CM000675.1:g.85032222T>C GRCh37
NC_000013.9:g.83930223T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104277T>C
XR_942133.1:n.369-46168A>G
XR_942134.1:n.366-46168A>G