ClinGen Allele Registry
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Canonical Allele Identifier:
CA337148595
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chrY:g.15732901C>G
GRCh37
chrY:g.17844781C>G
Linked Data - Sequence & Population
gnomAD v3:
Y:15732901 C / G
gnomAD v4:
chrY-15732901-C-G
Joint Max Group AF
0.98572882 (NFE)
Genomes Max Group AF
0.98572882 (NFE)
Linked Data - NCBI & NCI
dbSNP:
11799151
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.15732901C>G , CM000686.2:g.15732901C>G
GRCh38
NC_000024.9:g.17844781C>G , CM000686.1:g.17844781C>G
GRCh37
NC_000024.8:g.16354175C>G
NCBI36
Search 100 bp 5'
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