Canonical Allele Identifier: CA701680088

Gene: LINC00333

Linked Data

• dbSNP Id: rs1188339981
• MyVariant Identifiers: chr13:g.85032239T>G (hg19) ; chr13:g.84458104T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.84458104T>G , CM000675.2:g.84458104T>G	GRCh38
NC_000013.10:g.85032239T>G , CM000675.1:g.85032239T>G	GRCh37
NC_000013.9:g.83930240T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_046871.1:n.139-104260T>G
XR_942133.1:n.369-46185A>C
XR_942134.1:n.366-46185A>C