Canonical Allele Identifier: CA2360465131

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32805349C= , CM000682.2:g.32805349C=	GRCh38
NC_000020.10:g.31393155C= , CM000682.1:g.31393155C=	GRCh37
NC_000020.9:g.30856816C=	NCBI36
NG_007290.1:g.47965C= , LRG_56:g.47965C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1194C=	ENSP00000512497.1:n.*1194C=
ENST00000696232.1:c.2232-2413C=	ENSP00000512498.1:n.2232-2413C=
ENST00000696233.1:c.*975-2413C=	ENSP00000512499.1:n.*975-2413C=
ENST00000696238.1:c.*986C=	ENSP00000512502.1:n.*986C=
ENST00000696239.1:c.2024C=	ENSP00000512503.1:p.Ala675=
ENST00000696245.1:n.327-860C=
ENST00000201963.3:c.2219C=	ENSP00000201963.3:p.Ala740=
ENST00000328111.6:c.2243C= MANE Select	ENSP00000328547.2:p.Ala748=
ENST00000348286.6:c.2172-2413C=	ENSP00000337764.2:n.2172-2413C=
ENST00000353855.6:c.2183C=	ENSP00000313397.4:p.Ala728=
ENST00000443239.7:c.2046-2413C=	ENSP00000403169.2:n.2046-2413C=
ENST00000456297.6:c.1944-2413C=	ENSP00000412305.1:n.1944-2413C=
NM_001207055.1:c.2046-2413C=	NP_001193984.1:n.2046-2413C=
NM_001207056.1:c.1944-2413C=	NP_001193985.1:n.1944-2413C=
NM_006892.3:c.2243C= , LRG_56t1:c.2243C=	NP_008823.1:p.Ala748=
NM_175848.1:c.2183C=	NP_787044.1:p.Ala728=
NM_175849.1:c.2172-2413C=	NP_787045.1:n.2172-2413C=
NM_175850.2:c.2219C=	NP_787046.1:p.Ala740=
XM_011528653.1:c.2208-2413C=	XP_011526955.1:n.2208-2413C=
XM_011528654.1:c.2082-2413C=	XP_011526956.1:n.2082-2413C=
XR_936510.1:n.2210C=
XR_936511.1:n.2199-2413C=
XR_936512.1:n.2085C=
XM_011528653.2:c.2208-2413C=	XP_011526955.1:n.2208-2413C=
XM_011528654.2:c.2082-2413C=	XP_011526956.1:n.2082-2413C=
XR_936510.2:n.2221C=
XR_936511.2:n.2210-2413C=
XR_936512.2:n.2097C=
NM_001207055.2:c.2046-2413C=	NP_001193984.1:n.2046-2413C=
NM_001207056.2:c.1944-2413C=	NP_001193985.1:n.1944-2413C=
NM_006892.4:c.2243C= MANE Select	NP_008823.1:p.Ala748=
NM_175848.2:c.2183C=	NP_787044.1:p.Ala728=
NM_175849.2:c.2172-2413C=	NP_787045.1:n.2172-2413C=
NM_175850.3:c.2219C=	NP_787046.1:p.Ala740=