Canonical Allele Identifier: CA481866331

Gene: UBE3B

Linked Data

• MyVariant Identifiers: chr12:g.109959102T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109521297T>G , CM000674.2:g.109521297T>G	GRCh38
NC_000012.11:g.109959102T>G , CM000674.1:g.109959102T>G	GRCh37
NC_000012.10:g.108443485T>G	NCBI36
NG_033898.1:g.48675T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342494.8:c.2226T>G MANE Select	ENSP00000340596.3:p.Val742=
ENST00000342494.7:c.2226T>G	ENSP00000340596.3:p.Val742=
ENST00000434735.6:c.2226T>G	ENSP00000391529.2:p.Val742=
ENST00000449510.6:c.*196T>G	ENSP00000395802.2:n.*196T>G
ENST00000538070.1:n.1742T>G
ENST00000539584.5:n.1750T>G
ENST00000539599.5:c.2226T>G	ENSP00000443131.1:p.Val742=
NM_130466.3:c.2226T>G	NP_569733.2:p.Val742=
NM_183415.2:c.2226T>G	NP_904324.1:p.Val742=
XM_005253987.1:c.2226T>G	XP_005254044.1:p.Val742=
XM_006719681.2:c.2226T>G	XP_006719744.1:p.Val742=
XM_006719682.1:c.2226T>G	XP_006719745.1:p.Val742=
XM_011538959.1:c.2226T>G	XP_011537261.1:p.Val742=
XM_011538960.1:c.2226T>G	XP_011537262.1:p.Val742=
XM_011538961.1:c.2226T>G	XP_011537263.1:p.Val742=
XM_011538962.1:c.2226T>G	XP_011537264.1:p.Val742=
XR_429118.2:n.3053T>G
XM_005253987.2:c.2226T>G	XP_005254044.1:p.Val742=
XM_006719681.3:c.2226T>G	XP_006719744.1:p.Val742=
XM_006719682.2:c.2226T>G	XP_006719745.1:p.Val742=
XM_011538959.2:c.2226T>G	XP_011537261.1:p.Val742=
XM_017020195.1:c.1647T>G	XP_016875684.1:p.Val549=
XM_024449269.1:c.1647T>G	XP_024305037.1:p.Val549=
XR_429118.3:n.3053T>G
XR_429119.4:n.3242T>G
NM_130466.4:c.2226T>G MANE Select	NP_569733.2:p.Val742=
NM_183415.3:c.2226T>G	NP_904324.1:p.Val742=