Canonical Allele Identifier: CA2652424095

Gene: DNMT3B

Linked Data

• gnomAD v4: 20-32808125-A-ACCGTGTTAG

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32808125_32808126insCCGTGTTAG , CM000682.2:g.32808125_32808126insCCGTGTTAG	GRCh38
NC_000020.10:g.31395931_31395932insCCGTGTTAG , CM000682.1:g.31395931_31395932insCCGTGTTAG	GRCh37
NC_000020.9:g.30859592_30859593insCCGTGTTAG	NCBI36
NG_007290.1:g.50741_50742insCCGTGTTAG , LRG_56:g.50741_50742insCCGTGTTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1735_*1736insCCGTGTTAG	ENSP00000512497.1:n.*1735_*1736insCCGTGTTAG
ENST00000696232.1:c.*222_*223insCCGTGTTAG	ENSP00000512498.1:n.*222_*223insCCGTGTTAG
ENST00000696233.1:c.*1338_*1339insCCGTGTTAG	ENSP00000512499.1:n.*1338_*1339insCCGTGTTAG
ENST00000696238.1:c.*1527_*1528insCCGTGTTAG	ENSP00000512502.1:n.*1527_*1528insCCGTGTTAG
ENST00000696245.1:n.809_810insCCGTGTTAG
ENST00000201963.3:c.*222_*223insCCGTGTTAG	ENSP00000201963.3:n.*222_*223insCCGTGTTAG
ENST00000328111.6:c.*222_*223insCCGTGTTAG MANE Select	ENSP00000328547.2:n.*222_*223insCCGTGTTAG
ENST00000348286.6:c.*222_*223insCCGTGTTAG	ENSP00000337764.2:n.*222_*223insCCGTGTTAG
ENST00000353855.6:c.*222_*223insCCGTGTTAG	ENSP00000313397.4:n.*222_*223insCCGTGTTAG
ENST00000443239.7:c.*222_*223insCCGTGTTAG	ENSP00000403169.2:n.*222_*223insCCGTGTTAG
NM_001207055.1:c.*222_*223insCCGTGTTAG	NP_001193984.1:n.*222_*223insCCGTGTTAG
NM_001207056.1:c.*222_*223insCCGTGTTAG	NP_001193985.1:n.*222_*223insCCGTGTTAG
NM_006892.3:c.*222_*223insCCGTGTTAG , LRG_56t1:c.*222_*223insCCGTGTTAG	NP_008823.1:n.*222_*223insCCGTGTTAG
NM_175848.1:c.*222_*223insCCGTGTTAG	NP_787044.1:n.*222_*223insCCGTGTTAG
NM_175849.1:c.*222_*223insCCGTGTTAG	NP_787045.1:n.*222_*223insCCGTGTTAG
NM_175850.2:c.*222_*223insCCGTGTTAG	NP_787046.1:n.*222_*223insCCGTGTTAG
XM_011528653.1:c.*222_*223insCCGTGTTAG	XP_011526955.1:n.*222_*223insCCGTGTTAG
XM_011528654.1:c.*222_*223insCCGTGTTAG	XP_011526956.1:n.*222_*223insCCGTGTTAG
XR_936511.1:n.2562_2563insCCGTGTTAG
XM_011528653.2:c.*222_*223insCCGTGTTAG	XP_011526955.1:n.*222_*223insCCGTGTTAG
XM_011528654.2:c.*222_*223insCCGTGTTAG	XP_011526956.1:n.*222_*223insCCGTGTTAG
XR_936511.2:n.2573_2574insCCGTGTTAG
NM_001207055.2:c.*222_*223insCCGTGTTAG	NP_001193984.1:n.*222_*223insCCGTGTTAG
NM_001207056.2:c.*222_*223insCCGTGTTAG	NP_001193985.1:n.*222_*223insCCGTGTTAG
NM_006892.4:c.*222_*223insCCGTGTTAG MANE Select	NP_008823.1:n.*222_*223insCCGTGTTAG
NM_175848.2:c.*222_*223insCCGTGTTAG	NP_787044.1:n.*222_*223insCCGTGTTAG
NM_175849.2:c.*222_*223insCCGTGTTAG	NP_787045.1:n.*222_*223insCCGTGTTAG
NM_175850.3:c.*222_*223insCCGTGTTAG	NP_787046.1:n.*222_*223insCCGTGTTAG