Canonical Allele Identifier: CA337744830
Gene:
MyVariant.info:
GRCh38 chrY:g.14203273C>T
GRCh37 chrY:g.16315153C>T
gnomAD v3:
Y:14203273 C / T
gnomAD v4:
chrY-14203273-C-T
Joint Max Group AF 0.26986539 (SAS)
Genomes Max Group AF 0.26986539 (SAS)
dbSNP:
17222146
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.14203273C>T , CM000686.2:g.14203273C>T GRCh38
NC_000024.9:g.16315153C>T , CM000686.1:g.16315153C>T GRCh37
NC_000024.8:g.14824547C>T NCBI36
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