Canonical Allele Identifier: CA254038915
Gene: LINC00333 HGNC NCBI

Linked Data

dbSNP Id: rs934764079
MyVariant Identifiers: chr13:g.85032450A>T (hg19) chr13:g.84458315A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.84458315A>T , CM000675.2:g.84458315A>T GRCh38
NC_000013.10:g.85032450A>T , CM000675.1:g.85032450A>T GRCh37
NC_000013.9:g.83930451A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046871.1:n.139-104049A>T
XR_942133.1:n.369-46396T>A
XR_942134.1:n.366-46396T>A
Search 100 bp 5'
Search 100 bp 3'