ClinGen Allele Registry
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Canonical Allele Identifier:
CA876208931
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.51486768T>C
Linked Data - Sequence & Population
gnomAD v3:
X:51486768 T / C
gnomAD v4:
chrX-51486768-T-C
Joint Max Group AF
0.00018564 (AMR)
Genomes Max Group AF
0.00018564 (AMR)
Linked Data - NCBI & NCI
dbSNP:
1437469296
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.51486768T>C , CM000685.2:g.51486768T>C
GRCh38
NC_000023.10:g.51229620T>C , CM000685.1:g.51229620T>C
GRCh37
NC_000023.9:g.51246360T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'