ClinGen Allele Registry
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Canonical Allele Identifier:
CA1940871574
Gene: LINC01153
HGNC
NCBI
Linked Data
dbSNP Id:
rs1850761230
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.121179905G>T , CM000672.2:g.121179905G>T
GRCh38
NC_000010.10:g.122939419G>T , CM000672.1:g.122939419G>T
GRCh37
NC_000010.9:g.122929409G>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_246197.2:n.684+933G>T
Search 100 bp 5'
Search 100 bp 3'