Canonical Allele Identifier: CA408593313

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31395705A>T (hg19) ; chr20:g.32807899A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807899A>T , CM000682.2:g.32807899A>T	GRCh38
NC_000020.10:g.31395705A>T , CM000682.1:g.31395705A>T	GRCh37
NC_000020.9:g.30859366A>T	NCBI36
NG_007290.1:g.50515A>T , LRG_56:g.50515A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1509A>T	ENSP00000512497.1:n.*1509A>T
ENST00000696232.1:c.2369A>T	ENSP00000512498.1:p.Glu790Val
ENST00000696233.1:c.*1112A>T	ENSP00000512499.1:n.*1112A>T
ENST00000696238.1:c.*1301A>T	ENSP00000512502.1:n.*1301A>T
ENST00000696239.1:c.2339A>T	ENSP00000512503.1:p.Glu780Val
ENST00000696245.1:n.583A>T
ENST00000201963.3:c.2534A>T	ENSP00000201963.3:p.Glu845Val
ENST00000328111.6:c.2558A>T MANE Select	ENSP00000328547.2:p.Glu853Val
ENST00000348286.6:c.2309A>T	ENSP00000337764.2:p.Glu770Val
ENST00000353855.6:c.2498A>T	ENSP00000313397.4:p.Glu833Val
ENST00000443239.7:c.2183A>T	ENSP00000403169.2:p.Glu728Val
ENST00000456297.6:c.2081A>T	ENSP00000412305.1:p.Glu694Val
NM_001207055.1:c.2183A>T	NP_001193984.1:p.Glu728Val
NM_001207056.1:c.2081A>T	NP_001193985.1:p.Glu694Val
NM_006892.3:c.2558A>T , LRG_56t1:c.2558A>T	NP_008823.1:p.Glu853Val
NM_175848.1:c.2498A>T	NP_787044.1:p.Glu833Val
NM_175849.1:c.2309A>T	NP_787045.1:p.Glu770Val
NM_175850.2:c.2534A>T	NP_787046.1:p.Glu845Val
XM_011528653.1:c.2345A>T	XP_011526955.1:p.Glu782Val
XM_011528654.1:c.2219A>T	XP_011526956.1:p.Glu740Val
XR_936511.1:n.2336A>T
XM_011528653.2:c.2345A>T	XP_011526955.1:p.Glu782Val
XM_011528654.2:c.2219A>T	XP_011526956.1:p.Glu740Val
XR_936511.2:n.2347A>T
NM_001207055.2:c.2183A>T	NP_001193984.1:p.Glu728Val
NM_001207056.2:c.2081A>T	NP_001193985.1:p.Glu694Val
NM_006892.4:c.2558A>T MANE Select	NP_008823.1:p.Glu853Val
NM_175848.2:c.2498A>T	NP_787044.1:p.Glu833Val
NM_175849.2:c.2309A>T	NP_787045.1:p.Glu770Val
NM_175850.3:c.2534A>T	NP_787046.1:p.Glu845Val