Canonical Allele Identifier: CA386643067

Gene: UBE3B

Linked Data

• gnomAD v4: 12-109521450-G-A
• MyVariant Identifiers: chr12:g.109959255G>A (hg19) ; chr12:g.109521450G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109521450G>A , CM000674.2:g.109521450G>A	GRCh38
NC_000012.11:g.109959255G>A , CM000674.1:g.109959255G>A	GRCh37
NC_000012.10:g.108443638G>A	NCBI36
NG_033898.1:g.48828G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342494.8:c.2263G>A MANE Select	ENSP00000340596.3:p.Gly755Arg
ENST00000342494.7:c.2263G>A	ENSP00000340596.3:p.Gly755Arg
ENST00000434735.6:c.2263G>A	ENSP00000391529.2:p.Gly755Arg
ENST00000449510.6:c.*233G>A	ENSP00000395802.2:n.*233G>A
ENST00000538070.1:n.1779G>A
ENST00000539584.5:n.1787G>A
ENST00000539599.5:c.2263G>A	ENSP00000443131.1:p.Gly755Arg
NM_130466.3:c.2263G>A	NP_569733.2:p.Gly755Arg
NM_183415.2:c.2263G>A	NP_904324.1:p.Gly755Arg
XM_005253987.1:c.2263G>A	XP_005254044.1:p.Gly755Arg
XM_006719681.2:c.2263G>A	XP_006719744.1:p.Gly755Arg
XM_006719682.1:c.2263G>A	XP_006719745.1:p.Gly755Arg
XM_011538959.1:c.2263G>A	XP_011537261.1:p.Gly755Arg
XM_011538960.1:c.2263G>A	XP_011537262.1:p.Gly755Arg
XM_011538961.1:c.2263G>A	XP_011537263.1:p.Gly755Arg
XM_011538962.1:c.2263G>A	XP_011537264.1:p.Gly755Arg
XR_429118.2:n.3090G>A
XM_005253987.2:c.2263G>A	XP_005254044.1:p.Gly755Arg
XM_006719681.3:c.2263G>A	XP_006719744.1:p.Gly755Arg
XM_006719682.2:c.2263G>A	XP_006719745.1:p.Gly755Arg
XM_011538959.2:c.2263G>A	XP_011537261.1:p.Gly755Arg
XM_017020195.1:c.1684G>A	XP_016875684.1:p.Gly562Arg
XM_024449269.1:c.1684G>A	XP_024305037.1:p.Gly562Arg
XR_429118.3:n.3090G>A
XR_429119.4:n.3279G>A
NM_130466.4:c.2263G>A MANE Select	NP_569733.2:p.Gly755Arg
NM_183415.3:c.2263G>A	NP_904324.1:p.Gly755Arg