ClinGen Allele Registry
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Canonical Allele Identifier:
CA641829360
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.51486765T>G
GRCh37
chrX:g.51229617T>G
Linked Data - Sequence & Population
gnomAD v2:
X:51229617 T / G
gnomAD v3:
X:51486765 T / G
gnomAD v4:
chrX-51486765-T-G
Joint Max Group AF
0.00006365 (AFR)
Genomes Max Group AF
0.00006365 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1302887930
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.51486765T>G , CM000685.2:g.51486765T>G
GRCh38
NC_000023.10:g.51229617T>G , CM000685.1:g.51229617T>G
GRCh37
NC_000023.9:g.51246357T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'