Canonical Allele Identifier: CA337716755
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs540231334
gnomAD v3: Y-12580201-C-T
gnomAD v4: Y-12580201-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12580201C>T , CM000686.2:g.12580201C>T GRCh38
NC_000024.9:g.14692135C>T , CM000686.1:g.14692135C>T GRCh37
NC_000024.8:g.13202155C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000457658.6:n.653+33951C>T