Canonical Allele Identifier: CA2360456951

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32787249C= , CM000682.2:g.32787249C=	GRCh38
NC_000020.10:g.31375055C= , CM000682.1:g.31375055C=	GRCh37
NC_000020.9:g.30838716C=	NCBI36
NG_007290.1:g.29865C= , LRG_56:g.29865C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.452C=	ENSP00000512497.1:p.Thr151=
ENST00000696232.1:c.452C=	ENSP00000512498.1:p.Thr151=
ENST00000696233.1:c.452C=	ENSP00000512499.1:p.Thr151=
ENST00000696234.1:n.436C=
ENST00000696235.1:c.326C=	ENSP00000512500.1:p.Thr109=
ENST00000696236.1:c.326C=	ENSP00000512501.1:p.Thr109=
ENST00000696237.1:n.558C=
ENST00000696238.1:c.452C=	ENSP00000512502.1:p.Thr151=
ENST00000696239.1:c.452C=	ENSP00000512503.1:p.Thr151=
ENST00000201963.3:c.488C=	ENSP00000201963.3:p.Thr163=
ENST00000328111.6:c.452C= MANE Select	ENSP00000328547.2:p.Thr151=
ENST00000348286.6:c.452C=	ENSP00000337764.2:p.Thr151=
ENST00000353855.6:c.452C=	ENSP00000313397.4:p.Thr151=
ENST00000443239.7:c.326C=	ENSP00000403169.2:p.Thr109=
ENST00000456297.6:c.224C=	ENSP00000412305.1:p.Thr75=
NM_001207055.1:c.326C=	NP_001193984.1:p.Thr109=
NM_001207056.1:c.224C=	NP_001193985.1:p.Thr75=
NM_006892.3:c.452C= , LRG_56t1:c.452C=	NP_008823.1:p.Thr151=
NM_175848.1:c.452C=	NP_787044.1:p.Thr151=
NM_175849.1:c.452C=	NP_787045.1:p.Thr151=
NM_175850.2:c.488C=	NP_787046.1:p.Thr163=
XM_011528653.1:c.488C=	XP_011526955.1:p.Thr163=
XM_011528654.1:c.362C=	XP_011526956.1:p.Thr121=
XR_936510.1:n.624C=
XR_936511.1:n.624C=
XR_936512.1:n.499C=
XM_011528653.2:c.488C=	XP_011526955.1:p.Thr163=
XM_011528654.2:c.362C=	XP_011526956.1:p.Thr121=
XR_936510.2:n.635C=
XR_936511.2:n.635C=
XR_936512.2:n.511C=
NM_001207055.2:c.326C=	NP_001193984.1:p.Thr109=
NM_001207056.2:c.224C=	NP_001193985.1:p.Thr75=
NM_006892.4:c.452C= MANE Select	NP_008823.1:p.Thr151=
NM_175848.2:c.452C=	NP_787044.1:p.Thr151=
NM_175849.2:c.452C=	NP_787045.1:p.Thr151=
NM_175850.3:c.488C=	NP_787046.1:p.Thr163=