Canonical Allele Identifier: CA337586976
Gene: PRKY HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.7379653A>T
GRCh37 chrY:g.7247694A>T
gnomAD v3:
Y:7379653 A / T
gnomAD v4:
chrY-7379653-A-T
Joint Max Group AF 0.04885937 (SAS)
Genomes Max Group AF 0.04885937 (SAS)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7379653A>T , CM000686.2:g.7379653A>T GRCh38
NC_000024.9:g.7247694A>T , CM000686.1:g.7247694A>T GRCh37
NC_000024.8:g.7307694A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000528056.5:n.5323A>T
NR_028062.1:n.5323A>T
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