Canonical Allele Identifier: CA2360466358

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32808172G= , CM000682.2:g.32808172G=	GRCh38
NC_000020.10:g.31395978G= , CM000682.1:g.31395978G=	GRCh37
NC_000020.9:g.30859639G=	NCBI36
NG_007290.1:g.50788G= , LRG_56:g.50788G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1782G=	ENSP00000512497.1:n.*1782G=
ENST00000696232.1:c.*269G=	ENSP00000512498.1:n.*269G=
ENST00000696233.1:c.*1385G=	ENSP00000512499.1:n.*1385G=
ENST00000696238.1:c.*1574G=	ENSP00000512502.1:n.*1574G=
ENST00000696245.1:n.856G=
ENST00000201963.3:c.*269G=	ENSP00000201963.3:n.*269G=
ENST00000328111.6:c.*269G= MANE Select	ENSP00000328547.2:n.*269G=
ENST00000348286.6:c.*269G=	ENSP00000337764.2:n.*269G=
ENST00000353855.6:c.*269G=	ENSP00000313397.4:n.*269G=
ENST00000443239.7:c.*269G=	ENSP00000403169.2:n.*269G=
NM_001207055.1:c.*269G=	NP_001193984.1:n.*269G=
NM_001207056.1:c.*269G=	NP_001193985.1:n.*269G=
NM_006892.3:c.*269G= , LRG_56t1:c.*269G=	NP_008823.1:n.*269G=
NM_175848.1:c.*269G=	NP_787044.1:n.*269G=
NM_175849.1:c.*269G=	NP_787045.1:n.*269G=
NM_175850.2:c.*269G=	NP_787046.1:n.*269G=
XM_011528653.1:c.*269G=	XP_011526955.1:n.*269G=
XM_011528654.1:c.*269G=	XP_011526956.1:n.*269G=
XR_936511.1:n.2609G=
XM_011528653.2:c.*269G=	XP_011526955.1:n.*269G=
XM_011528654.2:c.*269G=	XP_011526956.1:n.*269G=
XR_936511.2:n.2620G=
NM_001207055.2:c.*269G=	NP_001193984.1:n.*269G=
NM_001207056.2:c.*269G=	NP_001193985.1:n.*269G=
NM_006892.4:c.*269G= MANE Select	NP_008823.1:n.*269G=
NM_175848.2:c.*269G=	NP_787044.1:n.*269G=
NM_175849.2:c.*269G=	NP_787045.1:n.*269G=
NM_175850.3:c.*269G=	NP_787046.1:n.*269G=