Canonical Allele Identifier: CA701680098

Gene: LINC00333

Linked Data

• dbSNP Id: rs1336880360
• MyVariant Identifiers: chr13:g.85032267A>T (hg19) ; chr13:g.84458132A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.84458132A>T , CM000675.2:g.84458132A>T	GRCh38
NC_000013.10:g.85032267A>T , CM000675.1:g.85032267A>T	GRCh37
NC_000013.9:g.83930268A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_046871.1:n.139-104232A>T
XR_942133.1:n.369-46213T>A
XR_942134.1:n.366-46213T>A