Canonical Allele Identifier: CA337716195
Gene: USP9Y HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.12552697G>C
GRCh37 chrY:g.14664631G>C
gnomAD v3:
Y:12552697 G / C
gnomAD v4:
chrY-12552697-G-C
Joint Max Group AF 0.66621236 (AFR)
Genomes Max Group AF 0.66621236 (AFR)
dbSNP:
9786634
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12552697G>C , CM000686.2:g.12552697G>C GRCh38
NC_000024.9:g.14664631G>C , CM000686.1:g.14664631G>C GRCh37
NC_000024.8:g.13174651G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000457658.6:n.653+6447G>C
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