Canonical Allele Identifier: CA337598607
Gene:
MyVariant.info:
GRCh38 chrY:g.7944404T>C
GRCh37 chrY:g.7812445T>C
gnomAD v3:
Y:7944404 T / C
gnomAD v4:
chrY-7944404-T-C
Joint Max Group AF 0.55675757 (AFR)
Genomes Max Group AF 0.55675757 (AFR)
dbSNP:
9306846
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7944404T>C , CM000686.2:g.7944404T>C GRCh38
NC_000024.9:g.7812445T>C , CM000686.1:g.7812445T>C GRCh37
NC_000024.8:g.7872445T>C NCBI36
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