Canonical Allele Identifier: CA2360462831

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32800256T= , CM000682.2:g.32800256T=	GRCh38
NC_000020.10:g.31388062T= , CM000682.1:g.31388062T=	GRCh37
NC_000020.9:g.30851723T=	NCBI36
NG_007290.1:g.42872T= , LRG_56:g.42872T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*814T=	ENSP00000512497.1:n.*814T=
ENST00000696232.1:c.1863T=	ENSP00000512498.1:p.Asn621=
ENST00000696233.1:c.*606T=	ENSP00000512499.1:n.*606T=
ENST00000696235.1:c.*511T=	ENSP00000512500.1:n.*511T=
ENST00000696238.1:c.*606T=	ENSP00000512502.1:n.*606T=
ENST00000696239.1:c.1644T=	ENSP00000512503.1:p.Asn548=
ENST00000201963.3:c.1839T=	ENSP00000201963.3:p.Asn613=
ENST00000328111.6:c.1863T= MANE Select	ENSP00000328547.2:p.Asn621=
ENST00000348286.6:c.1803T=	ENSP00000337764.2:p.Asn601=
ENST00000353855.6:c.1803T=	ENSP00000313397.4:p.Asn601=
ENST00000443239.7:c.1677T=	ENSP00000403169.2:p.Asn559=
ENST00000456297.6:c.1575T=	ENSP00000412305.1:p.Asn525=
NM_001207055.1:c.1677T=	NP_001193984.1:p.Asn559=
NM_001207056.1:c.1575T=	NP_001193985.1:p.Asn525=
NM_006892.3:c.1863T= , LRG_56t1:c.1863T=	NP_008823.1:p.Asn621=
NM_175848.1:c.1803T=	NP_787044.1:p.Asn601=
NM_175849.1:c.1803T=	NP_787045.1:p.Asn601=
NM_175850.2:c.1839T=	NP_787046.1:p.Asn613=
XM_011528653.1:c.1839T=	XP_011526955.1:p.Asn613=
XM_011528654.1:c.1713T=	XP_011526956.1:p.Asn571=
XR_936510.1:n.1830T=
XR_936511.1:n.1830T=
XR_936512.1:n.1705T=
XM_011528653.2:c.1839T=	XP_011526955.1:p.Asn613=
XM_011528654.2:c.1713T=	XP_011526956.1:p.Asn571=
XR_936510.2:n.1841T=
XR_936511.2:n.1841T=
XR_936512.2:n.1717T=
NM_001207055.2:c.1677T=	NP_001193984.1:p.Asn559=
NM_001207056.2:c.1575T=	NP_001193985.1:p.Asn525=
NM_006892.4:c.1863T= MANE Select	NP_008823.1:p.Asn621=
NM_175848.2:c.1803T=	NP_787044.1:p.Asn601=
NM_175849.2:c.1803T=	NP_787045.1:p.Asn601=
NM_175850.3:c.1839T=	NP_787046.1:p.Asn613=