Canonical Allele Identifier: CA2107005028
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs1879682865

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458134A>G , CM000675.2:g.84458134A>G GRCh38
NC_000013.10:g.85032269A>G , CM000675.1:g.85032269A>G GRCh37
NC_000013.9:g.83930270A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046871.1:n.139-104230A>G
XR_942133.1:n.369-46215T>C
XR_942134.1:n.366-46215T>C