Canonical Allele Identifier: CA1139166198
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs2053434578
gnomAD v3: Y-12720535-G-T
gnomAD v4: Y-12720535-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12720535G>T , CM000686.2:g.12720535G>T GRCh38
NC_000024.9:g.14832468G>T , CM000686.1:g.14832468G>T GRCh37
NC_000024.8:g.13341862G>T NCBI36
NG_008311.1:g.24309G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.97-54G>T ENSP00000498372.1:n.97-54G>T
ENST00000338981.7:c.97-54G>T MANE Select ENSP00000342812.3:n.97-54G>T
ENST00000426564.6:n.109-54G>T
ENST00000493168.1:n.173-54G>T
NM_004654.3:c.97-54G>T NP_004645.2:n.97-54G>T
XM_011531469.1:c.97-54G>T XP_011529771.1:n.97-54G>T
XM_011531470.1:c.-138-54G>T XP_011529772.1:n.-138-54G>T
XM_017030078.2:c.97-54G>T XP_016885567.1:n.97-54G>T
NM_004654.4:c.97-54G>T MANE Select NP_004645.2:n.97-54G>T
Search 100 bp 5'
Search 100 bp 3'