Canonical Allele Identifier: CA2360462813

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32800217G= , CM000682.2:g.32800217G=	GRCh38
NC_000020.10:g.31388023G= , CM000682.1:g.31388023G=	GRCh37
NC_000020.9:g.30851684G=	NCBI36
NG_007290.1:g.42833G= , LRG_56:g.42833G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*775G=	ENSP00000512497.1:n.*775G=
ENST00000696232.1:c.1824G=	ENSP00000512498.1:p.Glu608=
ENST00000696233.1:c.*567G=	ENSP00000512499.1:n.*567G=
ENST00000696235.1:c.*472G=	ENSP00000512500.1:n.*472G=
ENST00000696238.1:c.*567G=	ENSP00000512502.1:n.*567G=
ENST00000696239.1:c.1605G=	ENSP00000512503.1:p.Glu535=
ENST00000201963.3:c.1800G=	ENSP00000201963.3:p.Glu600=
ENST00000328111.6:c.1824G= MANE Select	ENSP00000328547.2:p.Glu608=
ENST00000348286.6:c.1764G=	ENSP00000337764.2:p.Glu588=
ENST00000353855.6:c.1764G=	ENSP00000313397.4:p.Glu588=
ENST00000443239.7:c.1638G=	ENSP00000403169.2:p.Glu546=
ENST00000456297.6:c.1536G=	ENSP00000412305.1:p.Glu512=
NM_001207055.1:c.1638G=	NP_001193984.1:p.Glu546=
NM_001207056.1:c.1536G=	NP_001193985.1:p.Glu512=
NM_006892.3:c.1824G= , LRG_56t1:c.1824G=	NP_008823.1:p.Glu608=
NM_175848.1:c.1764G=	NP_787044.1:p.Glu588=
NM_175849.1:c.1764G=	NP_787045.1:p.Glu588=
NM_175850.2:c.1800G=	NP_787046.1:p.Glu600=
XM_011528653.1:c.1800G=	XP_011526955.1:p.Glu600=
XM_011528654.1:c.1674G=	XP_011526956.1:p.Glu558=
XR_936510.1:n.1791G=
XR_936511.1:n.1791G=
XR_936512.1:n.1666G=
XM_011528653.2:c.1800G=	XP_011526955.1:p.Glu600=
XM_011528654.2:c.1674G=	XP_011526956.1:p.Glu558=
XR_936510.2:n.1802G=
XR_936511.2:n.1802G=
XR_936512.2:n.1678G=
NM_001207055.2:c.1638G=	NP_001193984.1:p.Glu546=
NM_001207056.2:c.1536G=	NP_001193985.1:p.Glu512=
NM_006892.4:c.1824G= MANE Select	NP_008823.1:p.Glu608=
NM_175848.2:c.1764G=	NP_787044.1:p.Glu588=
NM_175849.2:c.1764G=	NP_787045.1:p.Glu588=
NM_175850.3:c.1800G=	NP_787046.1:p.Glu600=