Canonical Allele Identifier: CA958336080
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs1879684941

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458236del , CM000675.2:g.84458236del GRCh38
NC_000013.10:g.85032371del , CM000675.1:g.85032371del GRCh37
NC_000013.9:g.83930372del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046871.1:n.139-104128del
XR_942133.1:n.369-46315del
XR_942134.1:n.366-46315del