Canonical Allele Identifier: CA1139295834
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs1603191541
gnomAD v3: Y-12580394-C-T
gnomAD v4: Y-12580394-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12580394C>T , CM000686.2:g.12580394C>T GRCh38
NC_000024.9:g.14692328C>T , CM000686.1:g.14692328C>T GRCh37
NC_000024.8:g.13202348C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000457658.6:n.653+34144C>T