Canonical Allele Identifier: CA337268329
Gene:
MyVariant.info:
GRCh38 chrY:g.16965529A>G
GRCh37 chrY:g.19077409A>G
gnomAD v3:
Y:16965529 A / G
gnomAD v4:
chrY-16965529-A-G
Joint Max Group AF 0.00147259 (NFE)
Genomes Max Group AF 0.00147259 (NFE)
dbSNP:
13304625
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.16965529A>G , CM000686.2:g.16965529A>G GRCh38
NC_000024.9:g.19077409A>G , CM000686.1:g.19077409A>G GRCh37
NC_000024.8:g.17586803A>G NCBI36
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