Canonical Allele Identifier: CA386643213

Gene: UBE3B

Linked Data

• MyVariant Identifiers: chr12:g.109959293C>G (hg19) ; chr12:g.109521488C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109521488C>G , CM000674.2:g.109521488C>G	GRCh38
NC_000012.11:g.109959293C>G , CM000674.1:g.109959293C>G	GRCh37
NC_000012.10:g.108443676C>G	NCBI36
NG_033898.1:g.48866C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342494.8:c.2301C>G MANE Select	ENSP00000340596.3:p.Ile767Met
ENST00000342494.7:c.2301C>G	ENSP00000340596.3:p.Ile767Met
ENST00000434735.6:c.2301C>G	ENSP00000391529.2:p.Ile767Met
ENST00000449510.6:c.*271C>G	ENSP00000395802.2:n.*271C>G
ENST00000538070.1:n.1817C>G
ENST00000539584.5:n.1825C>G
ENST00000539599.5:c.2301C>G	ENSP00000443131.1:p.Ile767Met
NM_130466.3:c.2301C>G	NP_569733.2:p.Ile767Met
NM_183415.2:c.2301C>G	NP_904324.1:p.Ile767Met
XM_005253987.1:c.2301C>G	XP_005254044.1:p.Ile767Met
XM_006719681.2:c.2301C>G	XP_006719744.1:p.Ile767Met
XM_006719682.1:c.2301C>G	XP_006719745.1:p.Ile767Met
XM_011538959.1:c.2301C>G	XP_011537261.1:p.Ile767Met
XM_011538960.1:c.2301C>G	XP_011537262.1:p.Ile767Met
XM_011538961.1:c.2301C>G	XP_011537263.1:p.Ile767Met
XM_011538962.1:c.2301C>G	XP_011537264.1:p.Ile767Met
XR_429118.2:n.3128C>G
XM_005253987.2:c.2301C>G	XP_005254044.1:p.Ile767Met
XM_006719681.3:c.2301C>G	XP_006719744.1:p.Ile767Met
XM_006719682.2:c.2301C>G	XP_006719745.1:p.Ile767Met
XM_011538959.2:c.2301C>G	XP_011537261.1:p.Ile767Met
XM_017020195.1:c.1722C>G	XP_016875684.1:p.Ile574Met
XM_024449269.1:c.1722C>G	XP_024305037.1:p.Ile574Met
XR_429118.3:n.3128C>G
XR_429119.4:n.3317C>G
NM_130466.4:c.2301C>G MANE Select	NP_569733.2:p.Ile767Met
NM_183415.3:c.2301C>G	NP_904324.1:p.Ile767Met