Canonical Allele Identifier: CA337347319
Gene:
MyVariant.info:
GRCh38 chrY:g.10171182T>C
GRCh37 chrY:g.10008791T>C
gnomAD v3:
Y:10171182 T / C
gnomAD v4:
chrY-10171182-T-C
Joint Max Group AF 0.94912504 (EAS)
Genomes Max Group AF 0.94912504 (EAS)
dbSNP:
9785831
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.10171182T>C , CM000686.2:g.10171182T>C GRCh38
NC_000024.9:g.10008791T>C , CM000686.1:g.10008791T>C GRCh37
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