Canonical Allele Identifier: CA254038893

Gene: LINC00333

Linked Data

• dbSNP Id: rs140003681
• gnomAD v2: 13-85032255-G-T
• gnomAD v3: 13-84458120-G-T
• gnomAD v4: 13-84458120-G-T
• MyVariant Identifiers: chr13:g.85032255G>T (hg19) ; chr13:g.84458120G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.84458120G>T , CM000675.2:g.84458120G>T	GRCh38
NC_000013.10:g.85032255G>T , CM000675.1:g.85032255G>T	GRCh37
NC_000013.9:g.83930256G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_046871.1:n.139-104244G>T
XR_942133.1:n.369-46201C>A
XR_942134.1:n.366-46201C>A