Canonical Allele Identifier: CA2360465174

Gene: DNMT3B

Linked Data

• dbSNP Id: rs1981860619

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32805446_32805447dup , CM000682.2:g.32805446_32805447dup	GRCh38
NC_000020.10:g.31393252_31393253dup , CM000682.1:g.31393252_31393253dup	GRCh37
NC_000020.9:g.30856913_30856914dup	NCBI36
NG_007290.1:g.48062_48063dup , LRG_56:g.48062_48063dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1252+39_*1252+40dup	ENSP00000512497.1:n.*1252+39_*1252+40dup
ENST00000696232.1:c.2232-2316_2232-2315dup	ENSP00000512498.1:n.2232-2316_2232-2315dup
ENST00000696233.1:c.*975-2316_*975-2315dup	ENSP00000512499.1:n.*975-2316_*975-2315dup
ENST00000696238.1:c.*1044+39_*1044+40dup	ENSP00000512502.1:n.*1044+39_*1044+40dup
ENST00000696239.1:c.2082+39_2082+40dup	ENSP00000512503.1:n.2082+39_2082+40dup
ENST00000696245.1:n.327-763_327-762dup
ENST00000201963.3:c.2277+39_2277+40dup	ENSP00000201963.3:n.2277+39_2277+40dup
ENST00000328111.6:c.2301+39_2301+40dup MANE Select	ENSP00000328547.2:n.2301+39_2301+40dup
ENST00000348286.6:c.2172-2316_2172-2315dup	ENSP00000337764.2:n.2172-2316_2172-2315dup
ENST00000353855.6:c.2241+39_2241+40dup	ENSP00000313397.4:n.2241+39_2241+40dup
ENST00000443239.7:c.2046-2316_2046-2315dup	ENSP00000403169.2:n.2046-2316_2046-2315dup
ENST00000456297.6:c.1944-2316_1944-2315dup	ENSP00000412305.1:n.1944-2316_1944-2315dup
NM_001207055.1:c.2046-2316_2046-2315dup	NP_001193984.1:n.2046-2316_2046-2315dup
NM_001207056.1:c.1944-2316_1944-2315dup	NP_001193985.1:n.1944-2316_1944-2315dup
NM_006892.3:c.2301+39_2301+40dup , LRG_56t1:c.2301+39_2301+40dup	NP_008823.1:n.2301+39_2301+40dup
NM_175848.1:c.2241+39_2241+40dup	NP_787044.1:n.2241+39_2241+40dup
NM_175849.1:c.2172-2316_2172-2315dup	NP_787045.1:n.2172-2316_2172-2315dup
NM_175850.2:c.2277+39_2277+40dup	NP_787046.1:n.2277+39_2277+40dup
XM_011528653.1:c.2208-2316_2208-2315dup	XP_011526955.1:n.2208-2316_2208-2315dup
XM_011528654.1:c.2082-2316_2082-2315dup	XP_011526956.1:n.2082-2316_2082-2315dup
XR_936510.1:n.2268+39_2268+40dup
XR_936511.1:n.2199-2316_2199-2315dup
XR_936512.1:n.2143+39_2143+40dup
XM_011528653.2:c.2208-2316_2208-2315dup	XP_011526955.1:n.2208-2316_2208-2315dup
XM_011528654.2:c.2082-2316_2082-2315dup	XP_011526956.1:n.2082-2316_2082-2315dup
XR_936510.2:n.2279+39_2279+40dup
XR_936511.2:n.2210-2316_2210-2315dup
XR_936512.2:n.2155+39_2155+40dup
NM_001207055.2:c.2046-2316_2046-2315dup	NP_001193984.1:n.2046-2316_2046-2315dup
NM_001207056.2:c.1944-2316_1944-2315dup	NP_001193985.1:n.1944-2316_1944-2315dup
NM_006892.4:c.2301+39_2301+40dup MANE Select	NP_008823.1:n.2301+39_2301+40dup
NM_175848.2:c.2241+39_2241+40dup	NP_787044.1:n.2241+39_2241+40dup
NM_175849.2:c.2172-2316_2172-2315dup	NP_787045.1:n.2172-2316_2172-2315dup
NM_175850.3:c.2277+39_2277+40dup	NP_787046.1:n.2277+39_2277+40dup