Canonical Allele Identifier: CA701680131

Gene: LINC00333

Linked Data

• dbSNP Id: rs1267999482
• gnomAD v3: 13-84458278-C-CA
• gnomAD v4: 13-84458278-C-CA
• MyVariant Identifiers: chr13:g.85032413_85032414insA (hg19) ; chr13:g.84458278_84458279insA (hg38)

Genomic Alleles

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

Transcript Alleles

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