ClinGen Allele Registry
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Canonical Allele Identifier:
CA1088161023
Gene: LINC00951
HGNC
NCBI
Linked Data
dbSNP Id:
rs1762014757
gnomAD v3:
6-40354108-TG-T
gnomAD v4:
6-40354108-TG-T
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.40354112del , CM000668.2:g.40354112del
GRCh38
NC_000006.11:g.40321851del , CM000668.1:g.40321851del
GRCh37
NC_000006.10:g.40429829del
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_038887.1:n.1898del
Search 100 bp 5'
Search 100 bp 3'