Canonical Allele Identifier: CA2360466356

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32808164T= , CM000682.2:g.32808164T=	GRCh38
NC_000020.10:g.31395970T= , CM000682.1:g.31395970T=	GRCh37
NC_000020.9:g.30859631T=	NCBI36
NG_007290.1:g.50780T= , LRG_56:g.50780T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1774T=	ENSP00000512497.1:n.*1774T=
ENST00000696232.1:c.*261T=	ENSP00000512498.1:n.*261T=
ENST00000696233.1:c.*1377T=	ENSP00000512499.1:n.*1377T=
ENST00000696238.1:c.*1566T=	ENSP00000512502.1:n.*1566T=
ENST00000696245.1:n.848T=
ENST00000201963.3:c.*261T=	ENSP00000201963.3:n.*261T=
ENST00000328111.6:c.*261T= MANE Select	ENSP00000328547.2:n.*261T=
ENST00000348286.6:c.*261T=	ENSP00000337764.2:n.*261T=
ENST00000353855.6:c.*261T=	ENSP00000313397.4:n.*261T=
ENST00000443239.7:c.*261T=	ENSP00000403169.2:n.*261T=
NM_001207055.1:c.*261T=	NP_001193984.1:n.*261T=
NM_001207056.1:c.*261T=	NP_001193985.1:n.*261T=
NM_006892.3:c.*261T= , LRG_56t1:c.*261T=	NP_008823.1:n.*261T=
NM_175848.1:c.*261T=	NP_787044.1:n.*261T=
NM_175849.1:c.*261T=	NP_787045.1:n.*261T=
NM_175850.2:c.*261T=	NP_787046.1:n.*261T=
XM_011528653.1:c.*261T=	XP_011526955.1:n.*261T=
XM_011528654.1:c.*261T=	XP_011526956.1:n.*261T=
XR_936511.1:n.2601T=
XM_011528653.2:c.*261T=	XP_011526955.1:n.*261T=
XM_011528654.2:c.*261T=	XP_011526956.1:n.*261T=
XR_936511.2:n.2612T=
NM_001207055.2:c.*261T=	NP_001193984.1:n.*261T=
NM_001207056.2:c.*261T=	NP_001193985.1:n.*261T=
NM_006892.4:c.*261T= MANE Select	NP_008823.1:n.*261T=
NM_175848.2:c.*261T=	NP_787044.1:n.*261T=
NM_175849.2:c.*261T=	NP_787045.1:n.*261T=
NM_175850.3:c.*261T=	NP_787046.1:n.*261T=