Canonical Allele Identifier: CA10573069
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs751452536
ExAC: Y:14847923 G / A
gnomAD v2: Y-14847923-G-A
gnomAD v3: Y-12735989-G-A
gnomAD v4: Y-12735989-G-A
MyVariant Identifiers: chrY:g.14847923G>A (hg19) chrY:g.12735989G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12735989G>A , CM000686.2:g.12735989G>A GRCh38
NC_000024.9:g.14847923G>A , CM000686.1:g.14847923G>A GRCh37
NC_000024.8:g.13357317G>A NCBI36
NG_008311.1:g.39764G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.774-9G>A ENSP00000498372.1:n.774-9G>A
ENST00000338981.7:c.774-9G>A MANE Select ENSP00000342812.3:n.774-9G>A
ENST00000426564.6:n.786-9G>A
NM_004654.3:c.774-9G>A NP_004645.2:n.774-9G>A
XM_011531469.1:c.774-9G>A XP_011529771.1:n.774-9G>A
XM_011531470.1:c.540-9G>A XP_011529772.1:n.540-9G>A
XM_017030078.2:c.774-9G>A XP_016885567.1:n.774-9G>A
NM_004654.4:c.774-9G>A MANE Select NP_004645.2:n.774-9G>A
Search 100 bp 5'
Search 100 bp 3'