Canonical Allele Identifier: CA337762877
Gene:
MyVariant.info:
GRCh38 chrY:g.15062861A>T
GRCh37 chrY:g.17174741A>T
gnomAD v3:
Y:15062861 A / T
gnomAD v4:
chrY-15062861-A-T
Joint Max Group AF 0.13022933 (MID)
Genomes Max Group AF 0.04953005 (AMR)
dbSNP:
35190095
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.15062861A>T , CM000686.2:g.15062861A>T GRCh38
NC_000024.9:g.17174741A>T , CM000686.1:g.17174741A>T GRCh37
NC_000024.8:g.15684135A>T NCBI36
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