ClinGen Allele Registry
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Canonical Allele Identifier:
CA337763446
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.15089941C>T
GRCh37
chrY:g.17201821C>T
Linked Data - Sequence & Population
gnomAD v3:
Y:15089941 C / T
gnomAD v4:
chrY-15089941-C-T
Joint Max Group AF
0.0024123 (AFR)
Genomes Max Group AF
0.0024123 (AFR)
Linked Data - NCBI & NCI
dbSNP:
188411414
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.15089941C>T , CM000686.2:g.15089941C>T
GRCh38
NC_000024.9:g.17201821C>T , CM000686.1:g.17201821C>T
GRCh37
NC_000024.8:g.15711215C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'