Canonical Allele Identifier: CA481866007

Gene: UBE3B

Linked Data

• MyVariant Identifiers: chr12:g.109959284A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109521479A>C , CM000674.2:g.109521479A>C	GRCh38
NC_000012.11:g.109959284A>C , CM000674.1:g.109959284A>C	GRCh37
NC_000012.10:g.108443667A>C	NCBI36
NG_033898.1:g.48857A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342494.8:c.2292A>C MANE Select	ENSP00000340596.3:p.Thr764=
ENST00000342494.7:c.2292A>C	ENSP00000340596.3:p.Thr764=
ENST00000434735.6:c.2292A>C	ENSP00000391529.2:p.Thr764=
ENST00000449510.6:c.*262A>C	ENSP00000395802.2:n.*262A>C
ENST00000538070.1:n.1808A>C
ENST00000539584.5:n.1816A>C
ENST00000539599.5:c.2292A>C	ENSP00000443131.1:p.Thr764=
NM_130466.3:c.2292A>C	NP_569733.2:p.Thr764=
NM_183415.2:c.2292A>C	NP_904324.1:p.Thr764=
XM_005253987.1:c.2292A>C	XP_005254044.1:p.Thr764=
XM_006719681.2:c.2292A>C	XP_006719744.1:p.Thr764=
XM_006719682.1:c.2292A>C	XP_006719745.1:p.Thr764=
XM_011538959.1:c.2292A>C	XP_011537261.1:p.Thr764=
XM_011538960.1:c.2292A>C	XP_011537262.1:p.Thr764=
XM_011538961.1:c.2292A>C	XP_011537263.1:p.Thr764=
XM_011538962.1:c.2292A>C	XP_011537264.1:p.Thr764=
XR_429118.2:n.3119A>C
XM_005253987.2:c.2292A>C	XP_005254044.1:p.Thr764=
XM_006719681.3:c.2292A>C	XP_006719744.1:p.Thr764=
XM_006719682.2:c.2292A>C	XP_006719745.1:p.Thr764=
XM_011538959.2:c.2292A>C	XP_011537261.1:p.Thr764=
XM_017020195.1:c.1713A>C	XP_016875684.1:p.Thr571=
XM_024449269.1:c.1713A>C	XP_024305037.1:p.Thr571=
XR_429118.3:n.3119A>C
XR_429119.4:n.3308A>C
NM_130466.4:c.2292A>C MANE Select	NP_569733.2:p.Thr764=
NM_183415.3:c.2292A>C	NP_904324.1:p.Thr764=