Canonical Allele Identifier: CA2360446428

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32765121T= , CM000682.2:g.32765121T=	GRCh38
NC_000020.10:g.31352927T= , CM000682.1:g.31352927T=	GRCh37
NC_000020.9:g.30816588T=	NCBI36
NG_007290.1:g.7737T= , LRG_56:g.7737T=

Transcript Alleles

HGVS	Amino-acid Change
NM_006892.4:c.-7+2422T= MANE Select	NP_008823.1:n.-7+2422T=
ENST00000328111.6:c.-7+2422T= MANE Select	ENSP00000328547.2:n.-7+2422T=
NM_001207055.1:c.-7+2422T=	NP_001193984.1:n.-7+2422T=
NM_001207055.2:c.-7+2422T=	NP_001193984.1:n.-7+2422T=
NM_001207056.1:c.-7+2422T=	NP_001193985.1:n.-7+2422T=
NM_001207056.2:c.-7+2422T=	NP_001193985.1:n.-7+2422T=
NM_006892.3:c.-7+2422T= , LRG_56t1:c.-7+2422T=	NP_008823.1:n.-7+2422T=
NM_175848.1:c.-7+2422T=	NP_787044.1:n.-7+2422T=
NM_175848.2:c.-7+2422T=	NP_787044.1:n.-7+2422T=
NM_175849.1:c.-7+2422T=	NP_787045.1:n.-7+2422T=
NM_175849.2:c.-7+2422T=	NP_787045.1:n.-7+2422T=
ENST00000348286.6:c.-7+2422T=	ENSP00000337764.2:n.-7+2422T=
ENST00000353855.6:c.-7+2422T=	ENSP00000313397.4:n.-7+2422T=
ENST00000443239.7:c.-7+2422T=	ENSP00000403169.2:n.-7+2422T=
ENST00000456297.6:c.-7+2422T=	ENSP00000412305.1:n.-7+2422T=
ENST00000696231.1:c.-7+2422T=	ENSP00000512497.1:n.-7+2422T=
ENST00000696232.1:c.-7+2422T=	ENSP00000512498.1:n.-7+2422T=
ENST00000696233.1:c.-7+2422T=	ENSP00000512499.1:n.-7+2422T=
ENST00000696234.1:n.104+2422T=
ENST00000696235.1:c.-7+2422T=	ENSP00000512500.1:n.-7+2422T=
ENST00000696236.1:c.-7+2422T=	ENSP00000512501.1:n.-7+2422T=
ENST00000696237.1:n.100+2260T=