Canonical Allele Identifier: CA337278665
Gene:
MyVariant.info:
GRCh38 chrY:g.17067455T>C
GRCh37 chrY:g.19179335T>C
gnomAD v3:
Y:17067455 T / C
gnomAD v4:
chrY-17067455-T-C
Joint Max Group AF 0.26403608 (MID)
Genomes Max Group AF 0.12406695 (SAS)
dbSNP:
17315835
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.17067455T>C , CM000686.2:g.17067455T>C GRCh38
NC_000024.9:g.19179335T>C , CM000686.1:g.19179335T>C GRCh37
NC_000024.8:g.17688729T>C NCBI36
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