Canonical Allele Identifier: CA701680135

Gene: LINC00333

Linked Data

• dbSNP Id: rs1252685777
• MyVariant Identifiers: chr13:g.85032425C>T (hg19) ; chr13:g.84458290C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.84458290C>T , CM000675.2:g.84458290C>T	GRCh38
NC_000013.10:g.85032425C>T , CM000675.1:g.85032425C>T	GRCh37
NC_000013.9:g.83930426C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046871.1:n.139-104074C>T
XR_942133.1:n.369-46371G>A
XR_942134.1:n.366-46371G>A