Canonical Allele Identifier: CA337715961
Gene: USP9Y HGNC NCBI
SHROOM2P1 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.12541166C>T
GRCh37 chrY:g.14653101C>T
gnomAD v3:
Y:12541166 C / T
gnomAD v4:
chrY-12541166-C-T
Joint Max Group AF 0.00024266 (NFE)
Genomes Max Group AF 0.00002524 (NFE)
Exomes Max Group AF 0.00026406 (NFE)
dbSNP:
35816667
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12541166C>T , CM000686.2:g.12541166C>T GRCh38
NC_000024.9:g.14653101C>T , CM000686.1:g.14653101C>T GRCh37
NC_000024.8:g.13163111C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000457658.6:n.358+3159C>T (USP9Y)
ENST00000434773.1:n.236C>T (SHROOM2P1)
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