Canonical Allele Identifier: CA1139298656
Gene: USP9Y HGNC NCBI

Linked Data

gnomAD v3: Y-12587010-C-G
gnomAD v4: Y-12587010-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12587010C>G , CM000686.2:g.12587010C>G GRCh38
NC_000024.9:g.14698944C>G , CM000686.1:g.14698944C>G GRCh37
NC_000024.8:g.13208964C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000457658.6:n.653+40760C>G