Canonical Allele Identifier: CA337719877
Gene: USP9Y HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.12773434T>C
GRCh37 chrY:g.14885368T>C
gnomAD v3:
Y:12773434 T / C
gnomAD v4:
chrY-12773434-T-C
Joint Max Group AF 0.00891919 (AFR)
Genomes Max Group AF 0.00713565 (AFR)
Exomes Max Group AF 0.0120003 (AFR)
dbSNP:
35407486
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12773434T>C , CM000686.2:g.12773434T>C GRCh38
NC_000024.9:g.14885368T>C , CM000686.1:g.14885368T>C GRCh37
NC_000024.8:g.13394762T>C NCBI36
NG_008311.1:g.77209T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651177.1:c.1989-149T>C ENSP00000498372.1:n.1989-149T>C
ENST00000338981.7:c.1989-149T>C MANE Select ENSP00000342812.3:n.1989-149T>C
ENST00000426564.6:n.2001-149T>C
NM_004654.3:c.1989-149T>C NP_004645.2:n.1989-149T>C
XM_011531469.1:c.1989-149T>C XP_011529771.1:n.1989-149T>C
XM_011531470.1:c.1755-149T>C XP_011529772.1:n.1755-149T>C
XM_017030078.2:c.2004-149T>C XP_016885567.1:n.2004-149T>C
NM_004654.4:c.1989-149T>C MANE Select NP_004645.2:n.1989-149T>C
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