ClinGen Allele Registry
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Canonical Allele Identifier:
CA331270441
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.74352261A>G
GRCh37
chrX:g.73572096A>G
Linked Data - Sequence & Population
gnomAD v2:
X:73572096 A / G
gnomAD v3:
X:74352261 A / G
gnomAD v4:
chrX-74352261-A-G
Joint Max Group AF
0.91534014 (EAS)
Genomes Max Group AF
0.91534014 (EAS)
Linked Data - NCBI & NCI
dbSNP:
1263237
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.74352261A>G , CM000685.2:g.74352261A>G
GRCh38
NC_000023.10:g.73572096A>G , CM000685.1:g.73572096A>G
GRCh37
NC_000023.9:g.73488821A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'