Canonical Allele Identifier: CA408593058

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31395633T>G (hg19) ; chr20:g.32807827T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807827T>G , CM000682.2:g.32807827T>G	GRCh38
NC_000020.10:g.31395633T>G , CM000682.1:g.31395633T>G	GRCh37
NC_000020.9:g.30859294T>G	NCBI36
NG_007290.1:g.50443T>G , LRG_56:g.50443T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1437T>G	ENSP00000512497.1:n.*1437T>G
ENST00000696232.1:c.2297T>G	ENSP00000512498.1:p.Leu766Arg
ENST00000696233.1:c.*1040T>G	ENSP00000512499.1:n.*1040T>G
ENST00000696238.1:c.*1229T>G	ENSP00000512502.1:n.*1229T>G
ENST00000696239.1:c.2267T>G	ENSP00000512503.1:p.Leu756Arg
ENST00000696245.1:n.511T>G
ENST00000201963.3:c.2462T>G	ENSP00000201963.3:p.Leu821Arg
ENST00000328111.6:c.2486T>G MANE Select	ENSP00000328547.2:p.Leu829Arg
ENST00000348286.6:c.2237T>G	ENSP00000337764.2:p.Leu746Arg
ENST00000353855.6:c.2426T>G	ENSP00000313397.4:p.Leu809Arg
ENST00000443239.7:c.2111T>G	ENSP00000403169.2:p.Leu704Arg
ENST00000456297.6:c.2009T>G	ENSP00000412305.1:p.Leu670Arg
NM_001207055.1:c.2111T>G	NP_001193984.1:p.Leu704Arg
NM_001207056.1:c.2009T>G	NP_001193985.1:p.Leu670Arg
NM_006892.3:c.2486T>G , LRG_56t1:c.2486T>G	NP_008823.1:p.Leu829Arg
NM_175848.1:c.2426T>G	NP_787044.1:p.Leu809Arg
NM_175849.1:c.2237T>G	NP_787045.1:p.Leu746Arg
NM_175850.2:c.2462T>G	NP_787046.1:p.Leu821Arg
XM_011528653.1:c.2273T>G	XP_011526955.1:p.Leu758Arg
XM_011528654.1:c.2147T>G	XP_011526956.1:p.Leu716Arg
XR_936511.1:n.2264T>G
XM_011528653.2:c.2273T>G	XP_011526955.1:p.Leu758Arg
XM_011528654.2:c.2147T>G	XP_011526956.1:p.Leu716Arg
XR_936511.2:n.2275T>G
NM_001207055.2:c.2111T>G	NP_001193984.1:p.Leu704Arg
NM_001207056.2:c.2009T>G	NP_001193985.1:p.Leu670Arg
NM_006892.4:c.2486T>G MANE Select	NP_008823.1:p.Leu829Arg
NM_175848.2:c.2426T>G	NP_787044.1:p.Leu809Arg
NM_175849.2:c.2237T>G	NP_787045.1:p.Leu746Arg
NM_175850.3:c.2462T>G	NP_787046.1:p.Leu821Arg