Canonical Allele Identifier: CA701680069

Gene: LINC00333

Linked Data

• dbSNP Id: rs1329718317
• gnomAD v3: 13-84458027-G-C
• gnomAD v4: 13-84458027-G-C
• MyVariant Identifiers: chr13:g.85032162G>C (hg19) ; chr13:g.84458027G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.84458027G>C , CM000675.2:g.84458027G>C	GRCh38
NC_000013.10:g.85032162G>C , CM000675.1:g.85032162G>C	GRCh37
NC_000013.9:g.83930163G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046871.1:n.139-104337G>C
XR_942133.1:n.369-46108C>G
XR_942134.1:n.366-46108C>G