Canonical Allele Identifier: CA337577626
Gene:
MyVariant.info:
GRCh38 chrY:g.7160422G>T
GRCh37 chrY:g.7028463G>T
gnomAD v3:
Y:7160422 G / T
gnomAD v4:
chrY-7160422-G-T
Joint Max Group AF 0.57351969 (AFR)
Genomes Max Group AF 0.57351969 (AFR)
dbSNP:
9786918
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7160422G>T , CM000686.2:g.7160422G>T GRCh38
NC_000024.9:g.7028463G>T , CM000686.1:g.7028463G>T GRCh37
NC_000024.8:g.7088463G>T NCBI36
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