Canonical Allele Identifier: CA337716752
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs1056201404
MyVariant Identifiers: chrY:g.14692063G>A (hg19) chrY:g.12580129G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12580129G>A , CM000686.2:g.12580129G>A GRCh38
NC_000024.9:g.14692063G>A , CM000686.1:g.14692063G>A GRCh37
NC_000024.8:g.13202083G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000457658.6:n.653+33879G>A
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