Canonical Allele Identifier: CA2360465136

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32805365A= , CM000682.2:g.32805365A=	GRCh38
NC_000020.10:g.31393171A= , CM000682.1:g.31393171A=	GRCh37
NC_000020.9:g.30856832A=	NCBI36
NG_007290.1:g.47981A= , LRG_56:g.47981A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1210A=	ENSP00000512497.1:n.*1210A=
ENST00000696232.1:c.2232-2397A=	ENSP00000512498.1:n.2232-2397A=
ENST00000696233.1:c.*975-2397A=	ENSP00000512499.1:n.*975-2397A=
ENST00000696238.1:c.*1002A=	ENSP00000512502.1:n.*1002A=
ENST00000696239.1:c.2040A=	ENSP00000512503.1:p.Lys680=
ENST00000696245.1:n.327-844A=
ENST00000201963.3:c.2235A=	ENSP00000201963.3:p.Lys745=
ENST00000328111.6:c.2259A= MANE Select	ENSP00000328547.2:p.Lys753=
ENST00000348286.6:c.2172-2397A=	ENSP00000337764.2:n.2172-2397A=
ENST00000353855.6:c.2199A=	ENSP00000313397.4:p.Lys733=
ENST00000443239.7:c.2046-2397A=	ENSP00000403169.2:n.2046-2397A=
ENST00000456297.6:c.1944-2397A=	ENSP00000412305.1:n.1944-2397A=
NM_001207055.1:c.2046-2397A=	NP_001193984.1:n.2046-2397A=
NM_001207056.1:c.1944-2397A=	NP_001193985.1:n.1944-2397A=
NM_006892.3:c.2259A= , LRG_56t1:c.2259A=	NP_008823.1:p.Lys753=
NM_175848.1:c.2199A=	NP_787044.1:p.Lys733=
NM_175849.1:c.2172-2397A=	NP_787045.1:n.2172-2397A=
NM_175850.2:c.2235A=	NP_787046.1:p.Lys745=
XM_011528653.1:c.2208-2397A=	XP_011526955.1:n.2208-2397A=
XM_011528654.1:c.2082-2397A=	XP_011526956.1:n.2082-2397A=
XR_936510.1:n.2226A=
XR_936511.1:n.2199-2397A=
XR_936512.1:n.2101A=
XM_011528653.2:c.2208-2397A=	XP_011526955.1:n.2208-2397A=
XM_011528654.2:c.2082-2397A=	XP_011526956.1:n.2082-2397A=
XR_936510.2:n.2237A=
XR_936511.2:n.2210-2397A=
XR_936512.2:n.2113A=
NM_001207055.2:c.2046-2397A=	NP_001193984.1:n.2046-2397A=
NM_001207056.2:c.1944-2397A=	NP_001193985.1:n.1944-2397A=
NM_006892.4:c.2259A= MANE Select	NP_008823.1:p.Lys753=
NM_175848.2:c.2199A=	NP_787044.1:p.Lys733=
NM_175849.2:c.2172-2397A=	NP_787045.1:n.2172-2397A=
NM_175850.3:c.2235A=	NP_787046.1:p.Lys745=