ClinGen Allele Registry
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Canonical Allele Identifier:
CA15049148
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chrX:g.90033228C>A
GRCh37
chrX:g.89288227C>A
Linked Data - Sequence & Population
gnomAD v2:
X:89288227 C / A
gnomAD v3:
X:90033228 C / A
gnomAD v4:
chrX-90033228-C-A
Joint Max Group AF
0.27383228 (EAS)
Genomes Max Group AF
0.27383228 (EAS)
Linked Data - NCBI & NCI
dbSNP:
5941436
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.90033228C>A , CM000685.2:g.90033228C>A
GRCh38
NC_000023.10:g.89288227C>A , CM000685.1:g.89288227C>A
GRCh37
NC_000023.9:g.89174883C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'