Canonical Allele Identifier: CA337165722
Gene:
MyVariant.info:
GRCh38 chrY:g.15965136T>C
GRCh37 chrY:g.18077016T>C
gnomAD v3:
Y:15965136 T / C
gnomAD v4:
chrY-15965136-T-C
Joint Max Group AF 0.00500096 (AMR)
Genomes Max Group AF 0.00500096 (AMR)
dbSNP:
34986875
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.15965136T>C , CM000686.2:g.15965136T>C GRCh38
NC_000024.9:g.18077016T>C , CM000686.1:g.18077016T>C GRCh37
NC_000024.8:g.16586410T>C NCBI36
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