ClinGen Allele Registry
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Canonical Allele Identifier:
CA331736686
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chrX:g.79658774A>G
GRCh37
chrX:g.78914271A>G
Linked Data - Sequence & Population
gnomAD v2:
X:78914271 A / G
gnomAD v3:
X:79658774 A / G
gnomAD v4:
chrX-79658774-A-G
Joint Max Group AF
0.57674425 (SAS)
Genomes Max Group AF
0.57674425 (SAS)
Linked Data - NCBI & NCI
dbSNP:
5959408
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.79658774A>G , CM000685.2:g.79658774A>G
GRCh38
NC_000023.10:g.78914271A>G , CM000685.1:g.78914271A>G
GRCh37
NC_000023.9:g.78800927A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'