Canonical Allele Identifier: CA337626659
Gene:
MyVariant.info:
GRCh38 chrY:g.8765504C>T
GRCh37 chrY:g.8633545C>T
gnomAD v3:
Y:8765504 C / T
gnomAD v4:
chrY-8765504-C-T
Joint Max Group AF 0.94983567 (EAS)
Genomes Max Group AF 0.94983567 (EAS)
dbSNP:
3853052
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8765504C>T , CM000686.2:g.8765504C>T GRCh38
NC_000024.9:g.8633545C>T , CM000686.1:g.8633545C>T GRCh37
NC_000024.8:g.8693545C>T NCBI36
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