Canonical Allele Identifier: CA10573187
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs772390241
ExAC: Y:14889912 C / A
gnomAD v2: Y-14889912-C-A
MyVariant Identifiers: chrY:g.14889912C>A (hg19) chrY:g.12777978C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12777978C>A , CM000686.2:g.12777978C>A GRCh38
NC_000024.9:g.14889912C>A , CM000686.1:g.14889912C>A GRCh37
NC_000024.8:g.13399306C>A NCBI36
NG_008311.1:g.81753C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.2640-41C>A ENSP00000498372.1:n.2640-41C>A
ENST00000338981.7:c.2640-41C>A MANE Select ENSP00000342812.3:n.2640-41C>A
ENST00000426564.6:n.2652-41C>A
NM_004654.3:c.2640-41C>A NP_004645.2:n.2640-41C>A
XM_011531469.1:c.2640-41C>A XP_011529771.1:n.2640-41C>A
XM_011531470.1:c.2406-41C>A XP_011529772.1:n.2406-41C>A
XM_017030078.2:c.2655-41C>A XP_016885567.1:n.2655-41C>A
NM_004654.4:c.2640-41C>A MANE Select NP_004645.2:n.2640-41C>A
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