ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA332307293
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.89275066T>G
GRCh37
chrX:g.88530065T>G
Linked Data - Sequence & Population
gnomAD v2:
X:88530065 T / G
gnomAD v3:
X:89275066 T / G
gnomAD v4:
chrX-89275066-T-G
Joint Max Group AF
0.49554855 (SAS)
Genomes Max Group AF
0.49554855 (SAS)
Linked Data - NCBI & NCI
dbSNP:
5941160
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.89275066T>G , CM000685.2:g.89275066T>G
GRCh38
NC_000023.10:g.88530065T>G , CM000685.1:g.88530065T>G
GRCh37
NC_000023.9:g.88416721T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'