Canonical Allele Identifier: CA2360466333

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32808089C= , CM000682.2:g.32808089C=	GRCh38
NC_000020.10:g.31395895C= , CM000682.1:g.31395895C=	GRCh37
NC_000020.9:g.30859556C=	NCBI36
NG_007290.1:g.50705C= , LRG_56:g.50705C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1699C=	ENSP00000512497.1:n.*1699C=
ENST00000696232.1:c.*186C=	ENSP00000512498.1:n.*186C=
ENST00000696233.1:c.*1302C=	ENSP00000512499.1:n.*1302C=
ENST00000696238.1:c.*1491C=	ENSP00000512502.1:n.*1491C=
ENST00000696245.1:n.773C=
ENST00000201963.3:c.*186C=	ENSP00000201963.3:n.*186C=
ENST00000328111.6:c.*186C= MANE Select	ENSP00000328547.2:n.*186C=
ENST00000348286.6:c.*186C=	ENSP00000337764.2:n.*186C=
ENST00000353855.6:c.*186C=	ENSP00000313397.4:n.*186C=
ENST00000443239.7:c.*186C=	ENSP00000403169.2:n.*186C=
NM_001207055.1:c.*186C=	NP_001193984.1:n.*186C=
NM_001207056.1:c.*186C=	NP_001193985.1:n.*186C=
NM_006892.3:c.*186C= , LRG_56t1:c.*186C=	NP_008823.1:n.*186C=
NM_175848.1:c.*186C=	NP_787044.1:n.*186C=
NM_175849.1:c.*186C=	NP_787045.1:n.*186C=
NM_175850.2:c.*186C=	NP_787046.1:n.*186C=
XM_011528653.1:c.*186C=	XP_011526955.1:n.*186C=
XM_011528654.1:c.*186C=	XP_011526956.1:n.*186C=
XR_936511.1:n.2526C=
XM_011528653.2:c.*186C=	XP_011526955.1:n.*186C=
XM_011528654.2:c.*186C=	XP_011526956.1:n.*186C=
XR_936511.2:n.2537C=
NM_001207055.2:c.*186C=	NP_001193984.1:n.*186C=
NM_001207056.2:c.*186C=	NP_001193985.1:n.*186C=
NM_006892.4:c.*186C= MANE Select	NP_008823.1:n.*186C=
NM_175848.2:c.*186C=	NP_787044.1:n.*186C=
NM_175849.2:c.*186C=	NP_787045.1:n.*186C=
NM_175850.3:c.*186C=	NP_787046.1:n.*186C=