Canonical Allele Identifier: CA2003934269

Gene: USP2

Linked Data

• dbSNP Id: rs2195525

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119364694C>A , CM000673.2:g.119364694C>A	GRCh38
NC_000011.9:g.119235404C>A , CM000673.1:g.119235404C>A	GRCh37
NC_000011.8:g.118740614C>A	NCBI36
NG_029825.1:g.22033G>T
NG_029825.2:g.22033G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260187.7:c.775-4460G>T MANE Select	ENSP00000260187.2:n.775-4460G>T
ENST00000260187.6:c.775-4460G>T	ENSP00000260187.2:n.775-4460G>T
ENST00000455332.6:c.46-4460G>T	ENSP00000407842.2:n.46-4460G>T
NM_001243759.1:c.46-4460G>T	NP_001230688.1:n.46-4460G>T
NM_004205.4:c.775-4460G>T	NP_004196.4:n.775-4460G>T
XM_005271721.3:c.775-4460G>T	XP_005271778.1:n.775-4460G>T
XM_005271722.1:c.775-4460G>T	XP_005271779.1:n.775-4460G>T
XM_005271721.5:c.775-4460G>T	XP_005271778.1:n.775-4460G>T
XM_005271722.2:c.775-4460G>T	XP_005271779.1:n.775-4460G>T
NM_004205.5:c.775-4460G>T MANE Select	NP_004196.4:n.775-4460G>T
NM_001243759.2:c.46-4460G>T	NP_001230688.1:n.46-4460G>T