Canonical Allele Identifier: CA10573582
Gene: USP9Y HGNC NCBI

Linked Data

dbSNP Id: rs2032604
ExAC: Y:14969634 T / G
gnomAD v2: Y-14969634-T-G
gnomAD v3: Y-12857709-T-G
gnomAD v4: Y-12857709-T-G
MyVariant Identifiers: chrY:g.14969634T>G (hg19) chrY:g.12857709T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12857709T>G , CM000686.2:g.12857709T>G GRCh38
NC_000024.9:g.14969634T>G , CM000686.1:g.14969634T>G GRCh37
NC_000024.8:g.13479028T>G NCBI36
NG_008311.1:g.161475T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651177.1:c.7530+48T>G ENSP00000498372.1:n.7530+48T>G
ENST00000338981.7:c.7530+48T>G MANE Select ENSP00000342812.3:n.7530+48T>G
ENST00000426564.6:n.7557+48T>G
ENST00000453031.1:c.575+48T>G
ENST00000471409.1:n.849+48T>G
NM_004654.3:c.7530+48T>G NP_004645.2:n.7530+48T>G
XM_011531469.1:c.7530+48T>G XP_011529771.1:n.7530+48T>G
XM_011531470.1:c.7296+48T>G XP_011529772.1:n.7296+48T>G
XM_017030078.2:c.7545+48T>G XP_016885567.1:n.7545+48T>G
NM_004654.4:c.7530+48T>G MANE Select NP_004645.2:n.7530+48T>G
Search 100 bp 5'
Search 100 bp 3'