ClinGen Allele Registry
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Canonical Allele Identifier:
CA1314064488
Gene: LINC01473
HGNC
NCBI
Linked Data
dbSNP Id:
rs1447464021
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.186079960T>A , CM000664.2:g.186079960T>A
GRCh38
NC_000002.11:g.186944687T>A , CM000664.1:g.186944687T>A
GRCh37
NC_000002.10:g.186652932T>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_110218.1:n.172+1370A>T
Search 100 bp 5'
Search 100 bp 3'