ClinGen Allele Registry
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Canonical Allele Identifier:
CA330779949
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.67801708C>T
GRCh37
chrX:g.67021550C>T
Linked Data - Sequence & Population
gnomAD v2:
X:67021550 C / T
gnomAD v3:
X:67801708 C / T
gnomAD v4:
chrX-67801708-C-T
Joint Max Group AF
0.97026539 (EAS)
Genomes Max Group AF
0.97026539 (EAS)
Linked Data - NCBI & NCI
dbSNP:
5919432
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.67801708C>T , CM000685.2:g.67801708C>T
GRCh38
NC_000023.10:g.67021550C>T , CM000685.1:g.67021550C>T
GRCh37
NC_000023.9:g.66938275C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'