Canonical Allele Identifier: CA254038901
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs576252598
MyVariant Identifiers: chr13:g.85032302G>A (hg19) chr13:g.84458167G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458167G>A , CM000675.2:g.84458167G>A GRCh38
NC_000013.10:g.85032302G>A , CM000675.1:g.85032302G>A GRCh37
NC_000013.9:g.83930303G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104197G>A
XR_942133.1:n.369-46248C>T
XR_942134.1:n.366-46248C>T
Search 100 bp 5'
Search 100 bp 3'