Canonical Allele Identifier: CA2652424155

Gene: DNMT3B

Linked Data

• gnomAD v4: 20-32808171-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32808171T>G , CM000682.2:g.32808171T>G	GRCh38
NC_000020.10:g.31395977T>G , CM000682.1:g.31395977T>G	GRCh37
NC_000020.9:g.30859638T>G	NCBI36
NG_007290.1:g.50787T>G , LRG_56:g.50787T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1781T>G	ENSP00000512497.1:n.*1781T>G
ENST00000696232.1:c.*268T>G	ENSP00000512498.1:n.*268T>G
ENST00000696233.1:c.*1384T>G	ENSP00000512499.1:n.*1384T>G
ENST00000696238.1:c.*1573T>G	ENSP00000512502.1:n.*1573T>G
ENST00000696245.1:n.855T>G
ENST00000201963.3:c.*268T>G	ENSP00000201963.3:n.*268T>G
ENST00000328111.6:c.*268T>G MANE Select	ENSP00000328547.2:n.*268T>G
ENST00000348286.6:c.*268T>G	ENSP00000337764.2:n.*268T>G
ENST00000353855.6:c.*268T>G	ENSP00000313397.4:n.*268T>G
ENST00000443239.7:c.*268T>G	ENSP00000403169.2:n.*268T>G
NM_001207055.1:c.*268T>G	NP_001193984.1:n.*268T>G
NM_001207056.1:c.*268T>G	NP_001193985.1:n.*268T>G
NM_006892.3:c.*268T>G , LRG_56t1:c.*268T>G	NP_008823.1:n.*268T>G
NM_175848.1:c.*268T>G	NP_787044.1:n.*268T>G
NM_175849.1:c.*268T>G	NP_787045.1:n.*268T>G
NM_175850.2:c.*268T>G	NP_787046.1:n.*268T>G
XM_011528653.1:c.*268T>G	XP_011526955.1:n.*268T>G
XM_011528654.1:c.*268T>G	XP_011526956.1:n.*268T>G
XR_936511.1:n.2608T>G
XM_011528653.2:c.*268T>G	XP_011526955.1:n.*268T>G
XM_011528654.2:c.*268T>G	XP_011526956.1:n.*268T>G
XR_936511.2:n.2619T>G
NM_001207055.2:c.*268T>G	NP_001193984.1:n.*268T>G
NM_001207056.2:c.*268T>G	NP_001193985.1:n.*268T>G
NM_006892.4:c.*268T>G MANE Select	NP_008823.1:n.*268T>G
NM_175848.2:c.*268T>G	NP_787044.1:n.*268T>G
NM_175849.2:c.*268T>G	NP_787045.1:n.*268T>G
NM_175850.3:c.*268T>G	NP_787046.1:n.*268T>G