ClinGen Allele Registry
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Canonical Allele Identifier:
CA991159735
Gene: LINC01924
HGNC
NCBI
Linked Data
dbSNP Id:
rs1599264082
gnomAD v3:
18-64209782-G-T
gnomAD v4:
18-64209782-G-T
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.64209782G>T , CM000680.2:g.64209782G>T
GRCh38
NC_000018.9:g.61877017G>T , CM000680.1:g.61877017G>T
GRCh37
NC_000018.8:g.60027997G>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_033881.1:n.201-39519G>T
Search 100 bp 5'
Search 100 bp 3'