Canonical Allele Identifier: CA337719251
Gene: USP9Y HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2032597

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12735858A>C , CM000686.2:g.12735858A>C GRCh38
NC_000024.9:g.14847792A>C , CM000686.1:g.14847792A>C GRCh37
NC_000024.8:g.13357186A>C NCBI36
NG_008311.1:g.39633A>C

Transcript Alleles

HGVS Amino-acid change
NM_004654.3:c.773+131A>C VV NP_004645.2:p.=
XM_011531469.1:c.773+131A>C XP_011529771.1:p.=
XM_011531470.1:c.539+65A>C XP_011529772.1:p.=
XM_017030078.2:c.773+131A>C XP_016885567.1:p.=
ENST00000338981.7:c.773+131A>C ENSP00000342812.3:p.=
ENST00000426564.6:n.785+131A>C