Canonical Allele Identifier: CA254038909

Gene: LINC00333

Linked Data

• dbSNP Id: rs926490934
• MyVariant Identifiers: chr13:g.85032392G>A (hg19) ; chr13:g.84458257G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.84458257G>A , CM000675.2:g.84458257G>A	GRCh38
NC_000013.10:g.85032392G>A , CM000675.1:g.85032392G>A	GRCh37
NC_000013.9:g.83930393G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046871.1:n.139-104107G>A
XR_942133.1:n.369-46338C>T
XR_942134.1:n.366-46338C>T