Canonical Allele Identifier: CA1139295826
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs778914553
gnomAD v3: Y-12580393-G-T
gnomAD v4: Y-12580393-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12580393G>T , CM000686.2:g.12580393G>T GRCh38
NC_000024.9:g.14692327G>T , CM000686.1:g.14692327G>T GRCh37
NC_000024.8:g.13202347G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000457658.6:n.653+34143G>T