ClinGen Allele Registry
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Canonical Allele Identifier:
CA326605233
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.10263651G>T
GRCh37
chrX:g.10231691G>T
Linked Data - Sequence & Population
gnomAD v2:
X:10231691 G / T
gnomAD v3:
X:10263651 G / T
gnomAD v4:
chrX-10263651-G-T
Joint Max Group AF
0.32763009 (AFR)
Genomes Max Group AF
0.32763009 (AFR)
Linked Data - NCBI & NCI
dbSNP:
12388359
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.10263651G>T , CM000685.2:g.10263651G>T
GRCh38
NC_000023.10:g.10231691G>T , CM000685.1:g.10231691G>T
GRCh37
NC_000023.9:g.10191691G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'