Canonical Allele Identifier: CA2816163333

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32808132C>G , CM000682.2:g.32808132C>G	GRCh38
NC_000020.10:g.31395938C>G , CM000682.1:g.31395938C>G	GRCh37
NC_000020.9:g.30859599C>G	NCBI36
NG_007290.1:g.50748C>G , LRG_56:g.50748C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1742C>G	ENSP00000512497.1:n.*1742C>G
ENST00000696232.1:c.*229C>G	ENSP00000512498.1:n.*229C>G
ENST00000696233.1:c.*1345C>G	ENSP00000512499.1:n.*1345C>G
ENST00000696238.1:c.*1534C>G	ENSP00000512502.1:n.*1534C>G
ENST00000696245.1:n.816C>G
ENST00000201963.3:c.*229C>G	ENSP00000201963.3:n.*229C>G
ENST00000328111.6:c.*229C>G MANE Select	ENSP00000328547.2:n.*229C>G
ENST00000348286.6:c.*229C>G	ENSP00000337764.2:n.*229C>G
ENST00000353855.6:c.*229C>G	ENSP00000313397.4:n.*229C>G
ENST00000443239.7:c.*229C>G	ENSP00000403169.2:n.*229C>G
NM_001207055.1:c.*229C>G	NP_001193984.1:n.*229C>G
NM_001207056.1:c.*229C>G	NP_001193985.1:n.*229C>G
NM_006892.3:c.*229C>G , LRG_56t1:c.*229C>G	NP_008823.1:n.*229C>G
NM_175848.1:c.*229C>G	NP_787044.1:n.*229C>G
NM_175849.1:c.*229C>G	NP_787045.1:n.*229C>G
NM_175850.2:c.*229C>G	NP_787046.1:n.*229C>G
XM_011528653.1:c.*229C>G	XP_011526955.1:n.*229C>G
XM_011528654.1:c.*229C>G	XP_011526956.1:n.*229C>G
XR_936511.1:n.2569C>G
XM_011528653.2:c.*229C>G	XP_011526955.1:n.*229C>G
XM_011528654.2:c.*229C>G	XP_011526956.1:n.*229C>G
XR_936511.2:n.2580C>G
NM_001207055.2:c.*229C>G	NP_001193984.1:n.*229C>G
NM_001207056.2:c.*229C>G	NP_001193985.1:n.*229C>G
NM_006892.4:c.*229C>G MANE Select	NP_008823.1:n.*229C>G
NM_175848.2:c.*229C>G	NP_787044.1:n.*229C>G
NM_175849.2:c.*229C>G	NP_787045.1:n.*229C>G
NM_175850.3:c.*229C>G	NP_787046.1:n.*229C>G