ClinGen Allele Registry
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Canonical Allele Identifier:
CA330697232
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.67096282C>T
GRCh37
chrX:g.66316124C>T
Linked Data - Sequence & Population
gnomAD v2:
X:66316124 C / T
gnomAD v3:
X:67096282 C / T
gnomAD v4:
chrX-67096282-C-T
Joint Max Group AF
0.97034266 (EAS)
Genomes Max Group AF
0.97034266 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1511061
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.67096282C>T , CM000685.2:g.67096282C>T
GRCh38
NC_000023.10:g.66316124C>T , CM000685.1:g.66316124C>T
GRCh37
NC_000023.9:g.66232849C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'