Canonical Allele Identifier: CA2360456957

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32787262A= , CM000682.2:g.32787262A=	GRCh38
NC_000020.10:g.31375068A= , CM000682.1:g.31375068A=	GRCh37
NC_000020.9:g.30838729A=	NCBI36
NG_007290.1:g.29878A= , LRG_56:g.29878A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.465A=	ENSP00000512497.1:p.Gly155=
ENST00000696232.1:c.465A=	ENSP00000512498.1:p.Gly155=
ENST00000696233.1:c.465A=	ENSP00000512499.1:p.Gly155=
ENST00000696234.1:n.449A=
ENST00000696235.1:c.339A=	ENSP00000512500.1:p.Gly113=
ENST00000696236.1:c.339A=	ENSP00000512501.1:p.Gly113=
ENST00000696237.1:n.571A=
ENST00000696238.1:c.465A=	ENSP00000512502.1:p.Gly155=
ENST00000696239.1:c.465A=	ENSP00000512503.1:p.Gly155=
ENST00000201963.3:c.501A=	ENSP00000201963.3:p.Gly167=
ENST00000328111.6:c.465A= MANE Select	ENSP00000328547.2:p.Gly155=
ENST00000348286.6:c.465A=	ENSP00000337764.2:p.Gly155=
ENST00000353855.6:c.465A=	ENSP00000313397.4:p.Gly155=
ENST00000443239.7:c.339A=	ENSP00000403169.2:p.Gly113=
ENST00000456297.6:c.237A=	ENSP00000412305.1:p.Gly79=
NM_001207055.1:c.339A=	NP_001193984.1:p.Gly113=
NM_001207056.1:c.237A=	NP_001193985.1:p.Gly79=
NM_006892.3:c.465A= , LRG_56t1:c.465A=	NP_008823.1:p.Gly155=
NM_175848.1:c.465A=	NP_787044.1:p.Gly155=
NM_175849.1:c.465A=	NP_787045.1:p.Gly155=
NM_175850.2:c.501A=	NP_787046.1:p.Gly167=
XM_011528653.1:c.501A=	XP_011526955.1:p.Gly167=
XM_011528654.1:c.375A=	XP_011526956.1:p.Gly125=
XR_936510.1:n.637A=
XR_936511.1:n.637A=
XR_936512.1:n.512A=
XM_011528653.2:c.501A=	XP_011526955.1:p.Gly167=
XM_011528654.2:c.375A=	XP_011526956.1:p.Gly125=
XR_936510.2:n.648A=
XR_936511.2:n.648A=
XR_936512.2:n.524A=
NM_001207055.2:c.339A=	NP_001193984.1:p.Gly113=
NM_001207056.2:c.237A=	NP_001193985.1:p.Gly79=
NM_006892.4:c.465A= MANE Select	NP_008823.1:p.Gly155=
NM_175848.2:c.465A=	NP_787044.1:p.Gly155=
NM_175849.2:c.465A=	NP_787045.1:p.Gly155=
NM_175850.3:c.501A=	NP_787046.1:p.Gly167=