ClinGen Allele Registry
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Canonical Allele Identifier:
CA335713718
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.129655744A>C
GRCh37
chrX:g.128789721A>C
Linked Data - Sequence & Population
gnomAD v2:
X:128789721 A / C
gnomAD v3:
X:129655744 A / C
gnomAD v4:
chrX-129655744-A-C
Joint Max Group AF
0.35962846 (EAS)
Genomes Max Group AF
0.35962846 (EAS)
Linked Data - NCBI & NCI
dbSNP:
3761581
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.129655744A>C , CM000685.2:g.129655744A>C
GRCh38
NC_000023.10:g.128789721A>C , CM000685.1:g.128789721A>C
GRCh37
NC_000023.9:g.128617402A>C
NCBI36
NG_016718.1:g.4213T>G
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