Canonical Allele Identifier: CA2360456958

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32787264C= , CM000682.2:g.32787264C=	GRCh38
NC_000020.10:g.31375070C= , CM000682.1:g.31375070C=	GRCh37
NC_000020.9:g.30838731C=	NCBI36
NG_007290.1:g.29880C= , LRG_56:g.29880C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.467C=	ENSP00000512497.1:p.Thr156=
ENST00000696232.1:c.467C=	ENSP00000512498.1:p.Thr156=
ENST00000696233.1:c.467C=	ENSP00000512499.1:p.Thr156=
ENST00000696234.1:n.451C=
ENST00000696235.1:c.341C=	ENSP00000512500.1:p.Thr114=
ENST00000696236.1:c.341C=	ENSP00000512501.1:p.Thr114=
ENST00000696237.1:n.573C=
ENST00000696238.1:c.467C=	ENSP00000512502.1:p.Thr156=
ENST00000696239.1:c.467C=	ENSP00000512503.1:p.Thr156=
ENST00000201963.3:c.503C=	ENSP00000201963.3:p.Thr168=
ENST00000328111.6:c.467C= MANE Select	ENSP00000328547.2:p.Thr156=
ENST00000348286.6:c.467C=	ENSP00000337764.2:p.Thr156=
ENST00000353855.6:c.467C=	ENSP00000313397.4:p.Thr156=
ENST00000443239.7:c.341C=	ENSP00000403169.2:p.Thr114=
ENST00000456297.6:c.239C=	ENSP00000412305.1:p.Thr80=
NM_001207055.1:c.341C=	NP_001193984.1:p.Thr114=
NM_001207056.1:c.239C=	NP_001193985.1:p.Thr80=
NM_006892.3:c.467C= , LRG_56t1:c.467C=	NP_008823.1:p.Thr156=
NM_175848.1:c.467C=	NP_787044.1:p.Thr156=
NM_175849.1:c.467C=	NP_787045.1:p.Thr156=
NM_175850.2:c.503C=	NP_787046.1:p.Thr168=
XM_011528653.1:c.503C=	XP_011526955.1:p.Thr168=
XM_011528654.1:c.377C=	XP_011526956.1:p.Thr126=
XR_936510.1:n.639C=
XR_936511.1:n.639C=
XR_936512.1:n.514C=
XM_011528653.2:c.503C=	XP_011526955.1:p.Thr168=
XM_011528654.2:c.377C=	XP_011526956.1:p.Thr126=
XR_936510.2:n.650C=
XR_936511.2:n.650C=
XR_936512.2:n.526C=
NM_001207055.2:c.341C=	NP_001193984.1:p.Thr114=
NM_001207056.2:c.239C=	NP_001193985.1:p.Thr80=
NM_006892.4:c.467C= MANE Select	NP_008823.1:p.Thr156=
NM_175848.2:c.467C=	NP_787044.1:p.Thr156=
NM_175849.2:c.467C=	NP_787045.1:p.Thr156=
NM_175850.3:c.503C=	NP_787046.1:p.Thr168=