Canonical Allele Identifier: CA1139263879
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs2053529061
gnomAD v3: Y-12810521-T-G
gnomAD v4: Y-12810521-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12810521T>G , CM000686.2:g.12810521T>G GRCh38
NC_000024.9:g.14922456T>G , CM000686.1:g.14922456T>G GRCh37
NC_000024.8:g.13431850T>G NCBI36
NG_008311.1:g.114297T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.4093-151T>G ENSP00000498372.1:n.4093-151T>G
ENST00000338981.7:c.4093-151T>G MANE Select ENSP00000342812.3:n.4093-151T>G
ENST00000426564.6:n.4105-151T>G
NM_004654.3:c.4093-151T>G NP_004645.2:n.4093-151T>G
XM_011531469.1:c.4093-151T>G XP_011529771.1:n.4093-151T>G
XM_011531470.1:c.3859-151T>G XP_011529772.1:n.3859-151T>G
XM_017030078.2:c.4108-151T>G XP_016885567.1:n.4108-151T>G
NM_004654.4:c.4093-151T>G MANE Select NP_004645.2:n.4093-151T>G
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