Canonical Allele Identifier: CA2062452813
Gene: UBE3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109521527G= , CM000674.2:g.109521527G= GRCh38
NC_000012.11:g.109959332G= , CM000674.1:g.109959332G= GRCh37
NC_000012.10:g.108443715G= NCBI36
NG_033898.1:g.48905G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342494.8:c.2340G= MANE Select ENSP00000340596.3:p.Lys780=
ENST00000342494.7:c.2340G= ENSP00000340596.3:p.Lys780=
ENST00000434735.6:c.2340G= ENSP00000391529.2:p.Lys780=
ENST00000449510.6:c.*310G= ENSP00000395802.2:n.*310G=
ENST00000538070.1:n.1856G=
ENST00000539584.5:n.1864G=
ENST00000539599.5:c.2340G= ENSP00000443131.1:p.Lys780=
NM_130466.3:c.2340G= NP_569733.2:p.Lys780=
NM_183415.2:c.2340G= NP_904324.1:p.Lys780=
XM_005253987.1:c.2340G= XP_005254044.1:p.Lys780=
XM_006719681.2:c.2340G= XP_006719744.1:p.Lys780=
XM_006719682.1:c.2340G= XP_006719745.1:p.Lys780=
XM_011538959.1:c.2340G= XP_011537261.1:p.Lys780=
XM_011538960.1:c.2340G= XP_011537262.1:p.Lys780=
XM_011538961.1:c.2340G= XP_011537263.1:p.Lys780=
XM_011538962.1:c.2340G= XP_011537264.1:p.Lys780=
XR_429118.2:n.3167G=
XM_005253987.2:c.2340G= XP_005254044.1:p.Lys780=
XM_006719681.3:c.2340G= XP_006719744.1:p.Lys780=
XM_006719682.2:c.2340G= XP_006719745.1:p.Lys780=
XM_011538959.2:c.2340G= XP_011537261.1:p.Lys780=
XM_017020195.1:c.1761G= XP_016875684.1:p.Lys587=
XM_024449269.1:c.1761G= XP_024305037.1:p.Lys587=
XR_429118.3:n.3167G=
XR_429119.4:n.3356G=
NM_130466.4:c.2340G= MANE Select NP_569733.2:p.Lys780=
NM_183415.3:c.2340G= NP_904324.1:p.Lys780=