ClinGen Allele Registry
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Canonical Allele Identifier:
CA991159753
Gene: LINC01924
HGNC
NCBI
Linked Data
dbSNP Id:
rs2051786429
gnomAD v3:
18-64209889-C-T
gnomAD v4:
18-64209889-C-T
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.64209889C>T , CM000680.2:g.64209889C>T
GRCh38
NC_000018.9:g.61877124C>T , CM000680.1:g.61877124C>T
GRCh37
NC_000018.8:g.60028104C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_033881.1:n.201-39412C>T
Search 100 bp 5'
Search 100 bp 3'