Canonical Allele Identifier: CA1139295839
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs2053357866
gnomAD v3: Y-12580415-A-G
gnomAD v4: Y-12580415-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12580415A>G , CM000686.2:g.12580415A>G GRCh38
NC_000024.9:g.14692349A>G , CM000686.1:g.14692349A>G GRCh37
NC_000024.8:g.13202369A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000457658.6:n.653+34165A>G