ClinGen Allele Registry
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Canonical Allele Identifier:
CA329467153
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.43747786T>G
GRCh37
chrX:g.43607033T>G
Linked Data - Sequence & Population
gnomAD v2:
X:43607033 T / G
gnomAD v3:
X:43747786 T / G
gnomAD v4:
chrX-43747786-T-G
Joint Max Group AF
0.24614663 (AFR)
Genomes Max Group AF
0.24614663 (AFR)
Linked Data - NCBI & NCI
dbSNP:
3027409
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.43747786T>G , CM000685.2:g.43747786T>G
GRCh38
NC_000023.10:g.43607033T>G , CM000685.1:g.43607033T>G
GRCh37
NC_000023.9:g.43491977T>G
NCBI36
NG_008957.2:g.96626T>G
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