ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA337588530
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.7455837C>T
GRCh37
chrY:g.7323878C>T
Linked Data - Sequence & Population
gnomAD v3:
Y:7455837 C / T
gnomAD v4:
chrY-7455837-C-T
Joint Max Group AF
0.27257683 (SAS)
Genomes Max Group AF
0.27257683 (SAS)
Linked Data - NCBI & NCI
dbSNP:
111508117
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.7455837C>T , CM000686.2:g.7455837C>T
GRCh38
NC_000024.9:g.7323878C>T , CM000686.1:g.7323878C>T
GRCh37
NC_000024.8:g.7383878C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'