Canonical Allele Identifier: CA337716756
Gene: USP9Y HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.12580293T>C
gnomAD v3:
Y:12580293 T / C
gnomAD v4:
chrY-12580293-T-C
Joint Max Group AF 0.07535266 (MID)
Genomes Max Group AF 0.03526704 (AMR)
dbSNP:
7892988
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12580293T>C , CM000686.2:g.12580293T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000457658.6:n.653+34043T>C
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