ClinGen Allele Registry
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Canonical Allele Identifier:
CA15010032
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chrX:g.86937000G>T
GRCh37
chrX:g.86192003G>T
Linked Data - Sequence & Population
gnomAD v2:
X:86192003 G / T
gnomAD v3:
X:86937000 G / T
gnomAD v4:
chrX-86937000-G-T
Joint Max Group AF
0.8258746 (AMR)
Genomes Max Group AF
0.8258746 (AMR)
Linked Data - NCBI & NCI
dbSNP:
2710057
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.86937000G>T , CM000685.2:g.86937000G>T
GRCh38
NC_000023.10:g.86192003G>T , CM000685.1:g.86192003G>T
GRCh37
NC_000023.9:g.86078659G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'