Canonical Allele Identifier: CA701680134

Gene: LINC00333

Linked Data

• dbSNP Id: rs1353697942
• gnomAD v3: 13-84458287-T-C
• gnomAD v4: 13-84458287-T-C
• MyVariant Identifiers: chr13:g.85032422T>C (hg19) ; chr13:g.84458287T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.84458287T>C , CM000675.2:g.84458287T>C	GRCh38
NC_000013.10:g.85032422T>C , CM000675.1:g.85032422T>C	GRCh37
NC_000013.9:g.83930423T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046871.1:n.139-104077T>C
XR_942133.1:n.369-46368A>G
XR_942134.1:n.366-46368A>G