Canonical Allele Identifier: CA920594851
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs1603191531

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12580204_12580205insAG , CM000686.2:g.12580204_12580205insAG GRCh38
NC_000024.9:g.14692138_14692139insAG , CM000686.1:g.14692138_14692139insAG GRCh37
NC_000024.8:g.13202158_13202159insAG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000457658.6:n.653+33954_653+33955insAG