Canonical Allele Identifier: CA337265457
Gene:
MyVariant.info:
GRCh38 chrY:g.16936722G>A
GRCh37 chrY:g.19048602G>A
gnomAD v3:
Y:16936722 G / A
gnomAD v4:
chrY-16936722-G-A
Joint Max Group AF 0.17470715 (NFE)
Genomes Max Group AF 0.17470715 (NFE)
dbSNP:
17249889
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.16936722G>A , CM000686.2:g.16936722G>A GRCh38
NC_000024.9:g.19048602G>A , CM000686.1:g.19048602G>A GRCh37
NC_000024.8:g.17557996G>A NCBI36
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