ClinGen Allele Registry
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Canonical Allele Identifier:
CA334740706
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.116435671G>A
Linked Data - Sequence & Population
gnomAD v3:
X:116435671 G / A
gnomAD v4:
chrX-116435671-G-A
Joint Max Group AF
0.72320397 (EAS)
Genomes Max Group AF
0.72320397 (EAS)
Linked Data - NCBI & NCI
dbSNP:
3788766
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.116435671G>A , CM000685.2:g.116435671G>A
GRCh38
NG_021305.2:g.4085G>A
Search 100 bp 5'
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