ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA14999382
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.1029445C>G
GRCh37
chrX:g.990180C>G
Linked Data - Sequence & Population
gnomAD v2:
X:990180 C / G
gnomAD v3:
X:1029445 C / G
gnomAD v4:
chrX-1029445-C-G
Joint Max Group AF
0.65642106 (NFE)
Genomes Max Group AF
0.65642106 (NFE)
Linked Data - NCBI & NCI
dbSNP:
4129148
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.1029445C>G , CM000685.2:g.1029445C>G
GRCh38
NC_000023.10:g.990180C>G , CM000685.1:g.990180C>G
GRCh37
NC_000023.9:g.910180C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'