ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA334645865
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.114583441G>C
Linked Data - Sequence & Population
gnomAD v3:
X:114583441 G / C
gnomAD v4:
chrX-114583441-G-C
Joint Max Group AF
0.00002621 (AFR)
Genomes Max Group AF
0.00002621 (AFR)
Linked Data - NCBI & NCI
dbSNP:
521018
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.114583441G>C , CM000685.2:g.114583441G>C
GRCh38
NG_012082.2:g.4357G>C
NG_012082.3:g.4357G>C
Search 100 bp 5'
Search 100 bp 3'