Canonical Allele Identifier: CA2360462833

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32800259C= , CM000682.2:g.32800259C=	GRCh38
NC_000020.10:g.31388065C= , CM000682.1:g.31388065C=	GRCh37
NC_000020.9:g.30851726C=	NCBI36
NG_007290.1:g.42875C= , LRG_56:g.42875C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*817C=	ENSP00000512497.1:n.*817C=
ENST00000696232.1:c.1866C=	ENSP00000512498.1:p.Ile622=
ENST00000696233.1:c.*609C=	ENSP00000512499.1:n.*609C=
ENST00000696235.1:c.*514C=	ENSP00000512500.1:n.*514C=
ENST00000696238.1:c.*609C=	ENSP00000512502.1:n.*609C=
ENST00000696239.1:c.1647C=	ENSP00000512503.1:p.Ile549=
ENST00000201963.3:c.1842C=	ENSP00000201963.3:p.Ile614=
ENST00000328111.6:c.1866C= MANE Select	ENSP00000328547.2:p.Ile622=
ENST00000348286.6:c.1806C=	ENSP00000337764.2:p.Ile602=
ENST00000353855.6:c.1806C=	ENSP00000313397.4:p.Ile602=
ENST00000443239.7:c.1680C=	ENSP00000403169.2:p.Ile560=
ENST00000456297.6:c.1578C=	ENSP00000412305.1:p.Ile526=
NM_001207055.1:c.1680C=	NP_001193984.1:p.Ile560=
NM_001207056.1:c.1578C=	NP_001193985.1:p.Ile526=
NM_006892.3:c.1866C= , LRG_56t1:c.1866C=	NP_008823.1:p.Ile622=
NM_175848.1:c.1806C=	NP_787044.1:p.Ile602=
NM_175849.1:c.1806C=	NP_787045.1:p.Ile602=
NM_175850.2:c.1842C=	NP_787046.1:p.Ile614=
XM_011528653.1:c.1842C=	XP_011526955.1:p.Ile614=
XM_011528654.1:c.1716C=	XP_011526956.1:p.Ile572=
XR_936510.1:n.1833C=
XR_936511.1:n.1833C=
XR_936512.1:n.1708C=
XM_011528653.2:c.1842C=	XP_011526955.1:p.Ile614=
XM_011528654.2:c.1716C=	XP_011526956.1:p.Ile572=
XR_936510.2:n.1844C=
XR_936511.2:n.1844C=
XR_936512.2:n.1720C=
NM_001207055.2:c.1680C=	NP_001193984.1:p.Ile560=
NM_001207056.2:c.1578C=	NP_001193985.1:p.Ile526=
NM_006892.4:c.1866C= MANE Select	NP_008823.1:p.Ile622=
NM_175848.2:c.1806C=	NP_787044.1:p.Ile602=
NM_175849.2:c.1806C=	NP_787045.1:p.Ile602=
NM_175850.3:c.1842C=	NP_787046.1:p.Ile614=