Canonical Allele Identifier: CA2360466221

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807871G= , CM000682.2:g.32807871G=	GRCh38
NC_000020.10:g.31395677G= , CM000682.1:g.31395677G=	GRCh37
NC_000020.9:g.30859338G=	NCBI36
NG_007290.1:g.50487G= , LRG_56:g.50487G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1481G=	ENSP00000512497.1:n.*1481G=
ENST00000696232.1:c.2341G=	ENSP00000512498.1:p.Ala781=
ENST00000696233.1:c.*1084G=	ENSP00000512499.1:n.*1084G=
ENST00000696238.1:c.*1273G=	ENSP00000512502.1:n.*1273G=
ENST00000696239.1:c.2311G=	ENSP00000512503.1:p.Ala771=
ENST00000696245.1:n.555G=
ENST00000201963.3:c.2506G=	ENSP00000201963.3:p.Ala836=
ENST00000328111.6:c.2530G= MANE Select	ENSP00000328547.2:p.Ala844=
ENST00000348286.6:c.2281G=	ENSP00000337764.2:p.Ala761=
ENST00000353855.6:c.2470G=	ENSP00000313397.4:p.Ala824=
ENST00000443239.7:c.2155G=	ENSP00000403169.2:p.Ala719=
ENST00000456297.6:c.2053G=	ENSP00000412305.1:p.Ala685=
NM_001207055.1:c.2155G=	NP_001193984.1:p.Ala719=
NM_001207056.1:c.2053G=	NP_001193985.1:p.Ala685=
NM_006892.3:c.2530G= , LRG_56t1:c.2530G=	NP_008823.1:p.Ala844=
NM_175848.1:c.2470G=	NP_787044.1:p.Ala824=
NM_175849.1:c.2281G=	NP_787045.1:p.Ala761=
NM_175850.2:c.2506G=	NP_787046.1:p.Ala836=
XM_011528653.1:c.2317G=	XP_011526955.1:p.Ala773=
XM_011528654.1:c.2191G=	XP_011526956.1:p.Ala731=
XR_936511.1:n.2308G=
XM_011528653.2:c.2317G=	XP_011526955.1:p.Ala773=
XM_011528654.2:c.2191G=	XP_011526956.1:p.Ala731=
XR_936511.2:n.2319G=
NM_001207055.2:c.2155G=	NP_001193984.1:p.Ala719=
NM_001207056.2:c.2053G=	NP_001193985.1:p.Ala685=
NM_006892.4:c.2530G= MANE Select	NP_008823.1:p.Ala844=
NM_175848.2:c.2470G=	NP_787044.1:p.Ala824=
NM_175849.2:c.2281G=	NP_787045.1:p.Ala761=
NM_175850.3:c.2506G=	NP_787046.1:p.Ala836=