Canonical Allele Identifier: CA10572388
Gene: PRKY HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.7367338G>A
GRCh37 chrY:g.7235379G>A
gnomAD v2:
Y:7235379 G / A
gnomAD v3:
Y:7367338 G / A
gnomAD v4:
chrY-7367338-G-A
Joint Max Group AF 0.00244278 (AFR)
Genomes Max Group AF 0.00055037 (AFR)
Exomes Max Group AF 0.00460893 (AFR)
dbSNP:
35195174
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7367338G>A , CM000686.2:g.7367338G>A GRCh38
NC_000024.9:g.7235379G>A , CM000686.1:g.7235379G>A GRCh37
NC_000024.8:g.7295379G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000528056.5:n.1157-18G>A
ENST00000533551.5:n.816-18G>A
NR_028062.1:n.1157-18G>A
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