Canonical Allele Identifier: CA337716754
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs550901455
gnomAD v3: Y-12580170-T-C
gnomAD v4: Y-12580170-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12580170T>C , CM000686.2:g.12580170T>C GRCh38
NC_000024.9:g.14692104T>C , CM000686.1:g.14692104T>C GRCh37
NC_000024.8:g.13202124T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000457658.6:n.653+33920T>C