ClinGen Allele Registry
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Canonical Allele Identifier:
CA334645877
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.114583649G>A
Linked Data - Sequence & Population
gnomAD v3:
X:114583649 G / A
gnomAD v4:
chrX-114583649-G-A
Joint Max Group AF
0.81991799 (EAS)
Genomes Max Group AF
0.81991799 (EAS)
Linked Data - NCBI & NCI
dbSNP:
498207
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.114583649G>A , CM000685.2:g.114583649G>A
GRCh38
NG_012082.2:g.4565G>A
NG_012082.3:g.4565G>A
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