Canonical Allele Identifier: CA337197962
Gene:
MyVariant.info:
GRCh38 chrY:g.16149674C>T
GRCh37 chrY:g.18261554C>T
gnomAD v3:
Y:16149674 C / T
gnomAD v4:
chrY-16149674-C-T
Joint Max Group AF 0.55233443 (AFR)
Genomes Max Group AF 0.55233443 (AFR)
dbSNP:
1019726
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.16149674C>T , CM000686.2:g.16149674C>T GRCh38
NC_000024.9:g.18261554C>T , CM000686.1:g.18261554C>T GRCh37
NC_000024.8:g.16770948C>T NCBI36
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