Canonical Allele Identifier: CA337716843
Gene: USP9Y HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.12586994C>T
gnomAD v3:
Y:12586994 C / T
gnomAD v4:
chrY-12586994-C-T
Joint Max Group AF 0.00250719 (NFE)
Genomes Max Group AF 0.00250719 (NFE)
dbSNP:
9786706
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12586994C>T , CM000686.2:g.12586994C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000457658.6:n.653+40744C>T
Search 100 bp 5'
Search 100 bp 3'