Canonical Allele Identifier: CA611350532
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs1267999482
gnomAD v2: 13-85032413-CA-C
gnomAD v3: 13-84458278-CA-C
gnomAD v4: 13-84458278-CA-C
MyVariant Identifiers: chr13:g.85032414del (hg19) chr13:g.84458279del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458286del , CM000675.2:g.84458286del GRCh38
NC_000013.10:g.85032421del , CM000675.1:g.85032421del GRCh37
NC_000013.9:g.83930422del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104078del
XR_942133.1:n.369-46360del
XR_942134.1:n.366-46360del
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