ClinGen Allele Registry
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Canonical Allele Identifier:
CA334645866
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.114583441G>T
Linked Data - Sequence & Population
gnomAD v3:
X:114583441 G / T
gnomAD v4:
chrX-114583441-G-T
Joint Max Group AF
0.82211481 (EAS)
Genomes Max Group AF
0.82211481 (EAS)
Linked Data - NCBI & NCI
dbSNP:
521018
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.114583441G>T , CM000685.2:g.114583441G>T
GRCh38
NG_012082.2:g.4357G>T
NG_012082.3:g.4357G>T
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