ClinGen Allele Registry
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Canonical Allele Identifier:
CA331603854
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chrX:g.78327951C>T
GRCh37
chrX:g.77583448C>T
Linked Data - Sequence & Population
gnomAD v2:
X:77583448 C / T
gnomAD v3:
X:78327951 C / T
gnomAD v4:
chrX-78327951-C-T
Joint Max Group AF
0.89491695 (AFR)
Genomes Max Group AF
0.89491695 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2806489
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.78327951C>T , CM000685.2:g.78327951C>T
GRCh38
NC_000023.10:g.77583448C>T , CM000685.1:g.77583448C>T
GRCh37
NC_000023.9:g.77470104C>T
NCBI36
NG_012809.1:g.4640G>A
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