Canonical Allele Identifier: CA337718082
Gene: USP9Y HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.12661223G>T
GRCh37 chrY:g.14773154G>T
gnomAD v3:
Y:12661223 G / T
gnomAD v4:
chrY-12661223-G-T
Joint Max Group AF 0.58293754 (AFR)
Genomes Max Group AF 0.58293754 (AFR)
dbSNP:
56095917
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12661223G>T , CM000686.2:g.12661223G>T GRCh38
NC_000024.9:g.14773154G>T , CM000686.1:g.14773154G>T GRCh37
NC_000024.8:g.13282548G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000457658.6:n.654-1133G>T
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