Canonical Allele Identifier: CA2360456947

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32787241G= , CM000682.2:g.32787241G=	GRCh38
NC_000020.10:g.31375047G= , CM000682.1:g.31375047G=	GRCh37
NC_000020.9:g.30838708G=	NCBI36
NG_007290.1:g.29857G= , LRG_56:g.29857G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.444G=	ENSP00000512497.1:p.Arg148=
ENST00000696232.1:c.444G=	ENSP00000512498.1:p.Arg148=
ENST00000696233.1:c.444G=	ENSP00000512499.1:p.Arg148=
ENST00000696234.1:n.428G=
ENST00000696235.1:c.318G=	ENSP00000512500.1:p.Arg106=
ENST00000696236.1:c.318G=	ENSP00000512501.1:p.Arg106=
ENST00000696237.1:n.550G=
ENST00000696238.1:c.444G=	ENSP00000512502.1:p.Arg148=
ENST00000696239.1:c.444G=	ENSP00000512503.1:p.Arg148=
ENST00000201963.3:c.480G=	ENSP00000201963.3:p.Arg160=
ENST00000328111.6:c.444G= MANE Select	ENSP00000328547.2:p.Arg148=
ENST00000348286.6:c.444G=	ENSP00000337764.2:p.Arg148=
ENST00000353855.6:c.444G=	ENSP00000313397.4:p.Arg148=
ENST00000443239.7:c.318G=	ENSP00000403169.2:p.Arg106=
ENST00000456297.6:c.216G=	ENSP00000412305.1:p.Arg72=
NM_001207055.1:c.318G=	NP_001193984.1:p.Arg106=
NM_001207056.1:c.216G=	NP_001193985.1:p.Arg72=
NM_006892.3:c.444G= , LRG_56t1:c.444G=	NP_008823.1:p.Arg148=
NM_175848.1:c.444G=	NP_787044.1:p.Arg148=
NM_175849.1:c.444G=	NP_787045.1:p.Arg148=
NM_175850.2:c.480G=	NP_787046.1:p.Arg160=
XM_011528653.1:c.480G=	XP_011526955.1:p.Arg160=
XM_011528654.1:c.354G=	XP_011526956.1:p.Arg118=
XR_936510.1:n.616G=
XR_936511.1:n.616G=
XR_936512.1:n.491G=
XM_011528653.2:c.480G=	XP_011526955.1:p.Arg160=
XM_011528654.2:c.354G=	XP_011526956.1:p.Arg118=
XR_936510.2:n.627G=
XR_936511.2:n.627G=
XR_936512.2:n.503G=
NM_001207055.2:c.318G=	NP_001193984.1:p.Arg106=
NM_001207056.2:c.216G=	NP_001193985.1:p.Arg72=
NM_006892.4:c.444G= MANE Select	NP_008823.1:p.Arg148=
NM_175848.2:c.444G=	NP_787044.1:p.Arg148=
NM_175849.2:c.444G=	NP_787045.1:p.Arg148=
NM_175850.3:c.480G=	NP_787046.1:p.Arg160=