Canonical Allele Identifier: CA371287655

Gene: UBXN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.58416949C>G , CM000670.2:g.58416949C>G	GRCh38
NC_000008.10:g.59329508C>G , CM000670.1:g.59329508C>G	GRCh37
NC_000008.9:g.59492062C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001077619.2:c.184C>G MANE Select	NP_001071087.1:p.Gln62Glu
ENST00000399598.7:c.184C>G MANE Select	ENSP00000382507.2:p.Gln62Glu
NM_001077619.1:c.184C>G	NP_001071087.1:p.Gln62Glu
NM_001330535.1:c.184C>G	NP_001317464.1:p.Gln62Glu
NM_001330535.2:c.184C>G	NP_001317464.1:p.Gln62Glu
NM_001363181.1:c.184C>G	NP_001350110.1:p.Gln62Glu
NR_156456.1:n.209C>G
ENST00000399598.6:c.184C>G	ENSP00000382507.2:p.Gln62Glu
ENST00000520732.5:c.184C>G	ENSP00000427759.1:p.Gln62Glu
ENST00000521796.1:c.20C>G
ENST00000522978.1:n.284C>G
ENST00000523409.5:c.184C>G	ENSP00000428314.1:p.Gln62Glu
XM_005251165.1:c.184C>G	XP_005251222.1:p.Gln62Glu
XM_005251166.1:c.184C>G	XP_005251223.1:p.Gln62Glu
XR_242453.1:n.209C>G