Canonical Allele Identifier: CA337592349
Gene:
MyVariant.info:
GRCh38 chrY:g.7678685G>A
GRCh37 chrY:g.7546726G>A
gnomAD v3:
Y:7678685 G / A
gnomAD v4:
chrY-7678685-G-A
Joint Max Group AF 0.09025911 (EAS)
Genomes Max Group AF 0.09025911 (EAS)
dbSNP:
2075181
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7678685G>A , CM000686.2:g.7678685G>A GRCh38
NC_000024.9:g.7546726G>A , CM000686.1:g.7546726G>A GRCh37
NC_000024.8:g.7606726G>A NCBI36
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