Canonical Allele Identifier: CA2360457009

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32787365C= , CM000682.2:g.32787365C=	GRCh38
NC_000020.10:g.31375171C= , CM000682.1:g.31375171C=	GRCh37
NC_000020.9:g.30838832C=	NCBI36
NG_007290.1:g.29981C= , LRG_56:g.29981C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.568C=	ENSP00000512497.1:p.Arg190=
ENST00000696232.1:c.568C=	ENSP00000512498.1:p.Arg190=
ENST00000696233.1:c.568C=	ENSP00000512499.1:p.Arg190=
ENST00000696234.1:n.552C=
ENST00000696235.1:c.442C=	ENSP00000512500.1:p.Arg148=
ENST00000696236.1:c.442C=	ENSP00000512501.1:p.Arg148=
ENST00000696237.1:n.674C=
ENST00000696238.1:c.568C=	ENSP00000512502.1:p.Arg190=
ENST00000696239.1:c.568C=	ENSP00000512503.1:p.Arg190=
ENST00000201963.3:c.604C=	ENSP00000201963.3:p.Arg202=
ENST00000328111.6:c.568C= MANE Select	ENSP00000328547.2:p.Arg190=
ENST00000348286.6:c.568C=	ENSP00000337764.2:p.Arg190=
ENST00000353855.6:c.568C=	ENSP00000313397.4:p.Arg190=
ENST00000443239.7:c.442C=	ENSP00000403169.2:p.Arg148=
ENST00000456297.6:c.340C=	ENSP00000412305.1:p.Arg114=
NM_001207055.1:c.442C=	NP_001193984.1:p.Arg148=
NM_001207056.1:c.340C=	NP_001193985.1:p.Arg114=
NM_006892.3:c.568C= , LRG_56t1:c.568C=	NP_008823.1:p.Arg190=
NM_175848.1:c.568C=	NP_787044.1:p.Arg190=
NM_175849.1:c.568C=	NP_787045.1:p.Arg190=
NM_175850.2:c.604C=	NP_787046.1:p.Arg202=
XM_011528653.1:c.604C=	XP_011526955.1:p.Arg202=
XM_011528654.1:c.478C=	XP_011526956.1:p.Arg160=
XR_936510.1:n.740C=
XR_936511.1:n.740C=
XR_936512.1:n.615C=
XM_011528653.2:c.604C=	XP_011526955.1:p.Arg202=
XM_011528654.2:c.478C=	XP_011526956.1:p.Arg160=
XR_936510.2:n.751C=
XR_936511.2:n.751C=
XR_936512.2:n.627C=
NM_001207055.2:c.442C=	NP_001193984.1:p.Arg148=
NM_001207056.2:c.340C=	NP_001193985.1:p.Arg114=
NM_006892.4:c.568C= MANE Select	NP_008823.1:p.Arg190=
NM_175848.2:c.568C=	NP_787044.1:p.Arg190=
NM_175849.2:c.568C=	NP_787045.1:p.Arg190=
NM_175850.3:c.604C=	NP_787046.1:p.Arg202=