ClinGen Allele Registry
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Canonical Allele Identifier:
CA700785460
Gene: LINC00393
HGNC
NCBI
Linked Data
dbSNP Id:
rs1183610386
gnomAD v3:
13-73492846-G-A
gnomAD v4:
13-73492846-G-A
MyVariant Identifiers:
chr13:g.74066983G>A (hg19)
chr13:g.73492846G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.73492846G>A , CM000675.2:g.73492846G>A
GRCh38
NC_000013.10:g.74066983G>A , CM000675.1:g.74066983G>A
GRCh37
NC_000013.9:g.72964984G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_942061.1:n.379-35884C>T
Search 100 bp 5'
Search 100 bp 3'