ClinGen Allele Registry
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Canonical Allele Identifier:
CA330699813
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.67116885C>A
GRCh37
chrX:g.66336727C>A
Linked Data - Sequence & Population
gnomAD v2:
X:66336727 C / A
gnomAD v3:
X:67116885 C / A
gnomAD v4:
chrX-67116885-C-A
Joint Max Group AF
0.97037017 (EAS)
Genomes Max Group AF
0.97037017 (EAS)
Linked Data - NCBI & NCI
dbSNP:
938059
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.67116885C>A , CM000685.2:g.67116885C>A
GRCh38
NC_000023.10:g.66336727C>A , CM000685.1:g.66336727C>A
GRCh37
NC_000023.9:g.66253452C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'