Canonical Allele Identifier: CA337647717
Gene:
MyVariant.info:
GRCh38 chrY:g.10041960T>C
GRCh37 chrY:g.9879569T>C
gnomAD v3:
Y:10041960 T / C
gnomAD v4:
chrY-10041960-T-C
Joint Max Group AF 0.04136446 (AFR)
Genomes Max Group AF 0.04136446 (AFR)
dbSNP:
9786637
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.10041960T>C , CM000686.2:g.10041960T>C GRCh38
NC_000024.9:g.9879569T>C , CM000686.1:g.9879569T>C GRCh37
NC_000024.8:g.10489569T>C NCBI36
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