Canonical Allele Identifier: CA611350535
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs1377093942
gnomAD v2: 13-85032429-GA-G
gnomAD v3: 13-84458294-GA-G
gnomAD v4: 13-84458294-GA-G
MyVariant Identifiers: chr13:g.85032430del (hg19) chr13:g.84458295del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458296del , CM000675.2:g.84458296del GRCh38
NC_000013.10:g.85032431del , CM000675.1:g.85032431del GRCh37
NC_000013.9:g.83930432del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104068del
XR_942133.1:n.369-46376del
XR_942134.1:n.366-46376del
Search 100 bp 5'
Search 100 bp 3'