Canonical Allele Identifier: CA337716756
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs7892988
gnomAD v3: Y-12580293-T-C
gnomAD v4: Y-12580293-T-C
MyVariant Identifiers: chrY:g.12580293T>C (hg38)
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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
Search 100 bp 5'
Search 100 bp 3'