Canonical Allele Identifier: CA337278666
Gene:
MyVariant.info:
GRCh38 chrY:g.17067583G>T
GRCh37 chrY:g.19179463G>T
gnomAD v3:
Y:17067583 G / T
gnomAD v4:
chrY-17067583-G-T
Joint Max Group AF 0.44149504 (EAS)
Genomes Max Group AF 0.44149504 (EAS)
dbSNP:
17276358
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.17067583G>T , CM000686.2:g.17067583G>T GRCh38
NC_000024.9:g.19179463G>T , CM000686.1:g.19179463G>T GRCh37
NC_000024.8:g.17688857G>T NCBI36
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