Canonical Allele Identifier: CA337716053
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs180966744
gnomAD v3: Y-12546187-G-A
gnomAD v4: Y-12546187-G-A
MyVariant Identifiers: chrY:g.14658122G>A (hg19) chrY:g.12546187G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12546187G>A , CM000686.2:g.12546187G>A GRCh38
NC_000024.9:g.14658122G>A , CM000686.1:g.14658122G>A GRCh37
NC_000024.8:g.13168132G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000457658.6:n.590G>A
Search 100 bp 5'
Search 100 bp 3'