Canonical Allele Identifier: CA254038899
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs983154858

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458153A>G , CM000675.2:g.84458153A>G GRCh38
NC_000013.10:g.85032288A>G , CM000675.1:g.85032288A>G GRCh37
NC_000013.9:g.83930289A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104211A>G
XR_942133.1:n.369-46234T>C
XR_942134.1:n.366-46234T>C