ClinGen Allele Registry
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Canonical Allele Identifier:
CA15056695
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.85840734G>A
GRCh37
chrX:g.85095739G>A
Linked Data - Sequence & Population
gnomAD v2:
X:85095739 G / A
gnomAD v3:
X:85840734 G / A
gnomAD v4:
chrX-85840734-G-A
Joint Max Group AF
0.36165002 (AFR)
Genomes Max Group AF
0.36165002 (AFR)
Linked Data - NCBI & NCI
dbSNP:
5967638
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.85840734G>A , CM000685.2:g.85840734G>A
GRCh38
NC_000023.10:g.85095739G>A , CM000685.1:g.85095739G>A
GRCh37
NC_000023.9:g.84982395G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'