Canonical Allele Identifier: CA337300047
Gene:
MyVariant.info:
GRCh38 chrY:g.17260928C>T
GRCh37 chrY:g.19372808C>T
gnomAD v3:
Y:17260928 C / T
gnomAD v4:
chrY-17260928-C-T
Joint Max Group AF 0.00207325 (NFE)
Genomes Max Group AF 0.00207325 (NFE)
dbSNP:
2215828
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.17260928C>T , CM000686.2:g.17260928C>T GRCh38
NC_000024.9:g.19372808C>T , CM000686.1:g.19372808C>T GRCh37
NC_000024.8:g.17882202C>T NCBI36
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