Canonical Allele Identifier: CA2360466251

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807933G= , CM000682.2:g.32807933G=	GRCh38
NC_000020.10:g.31395739G= , CM000682.1:g.31395739G=	GRCh37
NC_000020.9:g.30859400G=	NCBI36
NG_007290.1:g.50549G= , LRG_56:g.50549G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1543G=	ENSP00000512497.1:n.*1543G=
ENST00000696232.1:c.*30G=	ENSP00000512498.1:n.*30G=
ENST00000696233.1:c.*1146G=	ENSP00000512499.1:n.*1146G=
ENST00000696238.1:c.*1335G=	ENSP00000512502.1:n.*1335G=
ENST00000696245.1:n.617G=
ENST00000201963.3:c.*30G=	ENSP00000201963.3:n.*30G=
ENST00000328111.6:c.*30G= MANE Select	ENSP00000328547.2:n.*30G=
ENST00000348286.6:c.*30G=	ENSP00000337764.2:n.*30G=
ENST00000353855.6:c.*30G=	ENSP00000313397.4:n.*30G=
ENST00000443239.7:c.*30G=	ENSP00000403169.2:n.*30G=
ENST00000456297.6:c.*30G=	ENSP00000412305.1:n.*30G=
NM_001207055.1:c.*30G=	NP_001193984.1:n.*30G=
NM_001207056.1:c.*30G=	NP_001193985.1:n.*30G=
NM_006892.3:c.*30G= , LRG_56t1:c.*30G=	NP_008823.1:n.*30G=
NM_175848.1:c.*30G=	NP_787044.1:n.*30G=
NM_175849.1:c.*30G=	NP_787045.1:n.*30G=
NM_175850.2:c.*30G=	NP_787046.1:n.*30G=
XM_011528653.1:c.*30G=	XP_011526955.1:n.*30G=
XM_011528654.1:c.*30G=	XP_011526956.1:n.*30G=
XR_936511.1:n.2370G=
XM_011528653.2:c.*30G=	XP_011526955.1:n.*30G=
XM_011528654.2:c.*30G=	XP_011526956.1:n.*30G=
XR_936511.2:n.2381G=
NM_001207055.2:c.*30G=	NP_001193984.1:n.*30G=
NM_001207056.2:c.*30G=	NP_001193985.1:n.*30G=
NM_006892.4:c.*30G= MANE Select	NP_008823.1:n.*30G=
NM_175848.2:c.*30G=	NP_787044.1:n.*30G=
NM_175849.2:c.*30G=	NP_787045.1:n.*30G=
NM_175850.3:c.*30G=	NP_787046.1:n.*30G=