Canonical Allele Identifier: CA2360462817

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32800227G= , CM000682.2:g.32800227G=	GRCh38
NC_000020.10:g.31388033G= , CM000682.1:g.31388033G=	GRCh37
NC_000020.9:g.30851694G=	NCBI36
NG_007290.1:g.42843G= , LRG_56:g.42843G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*785G=	ENSP00000512497.1:n.*785G=
ENST00000696232.1:c.1834G=	ENSP00000512498.1:p.Ala612=
ENST00000696233.1:c.*577G=	ENSP00000512499.1:n.*577G=
ENST00000696235.1:c.*482G=	ENSP00000512500.1:n.*482G=
ENST00000696238.1:c.*577G=	ENSP00000512502.1:n.*577G=
ENST00000696239.1:c.1615G=	ENSP00000512503.1:p.Ala539=
ENST00000201963.3:c.1810G=	ENSP00000201963.3:p.Ala604=
ENST00000328111.6:c.1834G= MANE Select	ENSP00000328547.2:p.Ala612=
ENST00000348286.6:c.1774G=	ENSP00000337764.2:p.Ala592=
ENST00000353855.6:c.1774G=	ENSP00000313397.4:p.Ala592=
ENST00000443239.7:c.1648G=	ENSP00000403169.2:p.Ala550=
ENST00000456297.6:c.1546G=	ENSP00000412305.1:p.Ala516=
NM_001207055.1:c.1648G=	NP_001193984.1:p.Ala550=
NM_001207056.1:c.1546G=	NP_001193985.1:p.Ala516=
NM_006892.3:c.1834G= , LRG_56t1:c.1834G=	NP_008823.1:p.Ala612=
NM_175848.1:c.1774G=	NP_787044.1:p.Ala592=
NM_175849.1:c.1774G=	NP_787045.1:p.Ala592=
NM_175850.2:c.1810G=	NP_787046.1:p.Ala604=
XM_011528653.1:c.1810G=	XP_011526955.1:p.Ala604=
XM_011528654.1:c.1684G=	XP_011526956.1:p.Ala562=
XR_936510.1:n.1801G=
XR_936511.1:n.1801G=
XR_936512.1:n.1676G=
XM_011528653.2:c.1810G=	XP_011526955.1:p.Ala604=
XM_011528654.2:c.1684G=	XP_011526956.1:p.Ala562=
XR_936510.2:n.1812G=
XR_936511.2:n.1812G=
XR_936512.2:n.1688G=
NM_001207055.2:c.1648G=	NP_001193984.1:p.Ala550=
NM_001207056.2:c.1546G=	NP_001193985.1:p.Ala516=
NM_006892.4:c.1834G= MANE Select	NP_008823.1:p.Ala612=
NM_175848.2:c.1774G=	NP_787044.1:p.Ala592=
NM_175849.2:c.1774G=	NP_787045.1:p.Ala592=
NM_175850.3:c.1810G=	NP_787046.1:p.Ala604=