Canonical Allele Identifier: CA701680120

Gene: LINC00333

Linked Data

• dbSNP Id: rs1172895783
• MyVariant Identifiers: chr13:g.85032369C>T (hg19) ; chr13:g.84458234C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.84458234C>T , CM000675.2:g.84458234C>T	GRCh38
NC_000013.10:g.85032369C>T , CM000675.1:g.85032369C>T	GRCh37
NC_000013.9:g.83930370C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046871.1:n.139-104130C>T
XR_942133.1:n.369-46315G>A
XR_942134.1:n.366-46315G>A