Canonical Allele Identifier: CA408588835

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31388106T>G (hg19) ; chr20:g.32800300T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32800300T>G , CM000682.2:g.32800300T>G	GRCh38
NC_000020.10:g.31388106T>G , CM000682.1:g.31388106T>G	GRCh37
NC_000020.9:g.30851767T>G	NCBI36
NG_007290.1:g.42916T>G , LRG_56:g.42916T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*856+2T>G	ENSP00000512497.1:n.*856+2T>G
ENST00000696232.1:c.1905+2T>G	ENSP00000512498.1:n.1905+2T>G
ENST00000696233.1:c.*648+2T>G	ENSP00000512499.1:n.*648+2T>G
ENST00000696235.1:c.*553+2T>G	ENSP00000512500.1:n.*553+2T>G
ENST00000696238.1:c.*648+2T>G	ENSP00000512502.1:n.*648+2T>G
ENST00000696239.1:c.1686+2T>G	ENSP00000512503.1:n.1686+2T>G
ENST00000201963.3:c.1881+2T>G	ENSP00000201963.3:n.1881+2T>G
ENST00000328111.6:c.1905+2T>G MANE Select	ENSP00000328547.2:n.1905+2T>G
ENST00000348286.6:c.1845+2T>G	ENSP00000337764.2:n.1845+2T>G
ENST00000353855.6:c.1845+2T>G	ENSP00000313397.4:n.1845+2T>G
ENST00000443239.7:c.1719+2T>G	ENSP00000403169.2:n.1719+2T>G
ENST00000456297.6:c.1617+2T>G	ENSP00000412305.1:n.1617+2T>G
NM_001207055.1:c.1719+2T>G	NP_001193984.1:n.1719+2T>G
NM_001207056.1:c.1617+2T>G	NP_001193985.1:n.1617+2T>G
NM_006892.3:c.1905+2T>G , LRG_56t1:c.1905+2T>G	NP_008823.1:n.1905+2T>G
NM_175848.1:c.1845+2T>G	NP_787044.1:n.1845+2T>G
NM_175849.1:c.1845+2T>G	NP_787045.1:n.1845+2T>G
NM_175850.2:c.1881+2T>G	NP_787046.1:n.1881+2T>G
XM_011528653.1:c.1881+2T>G	XP_011526955.1:n.1881+2T>G
XM_011528654.1:c.1755+2T>G	XP_011526956.1:n.1755+2T>G
XR_936510.1:n.1872+2T>G
XR_936511.1:n.1872+2T>G
XR_936512.1:n.1747+2T>G
XM_011528653.2:c.1881+2T>G	XP_011526955.1:n.1881+2T>G
XM_011528654.2:c.1755+2T>G	XP_011526956.1:n.1755+2T>G
XR_936510.2:n.1883+2T>G
XR_936511.2:n.1883+2T>G
XR_936512.2:n.1759+2T>G
NM_001207055.2:c.1719+2T>G	NP_001193984.1:n.1719+2T>G
NM_001207056.2:c.1617+2T>G	NP_001193985.1:n.1617+2T>G
NM_006892.4:c.1905+2T>G MANE Select	NP_008823.1:n.1905+2T>G
NM_175848.2:c.1845+2T>G	NP_787044.1:n.1845+2T>G
NM_175849.2:c.1845+2T>G	NP_787045.1:n.1845+2T>G
NM_175850.3:c.1881+2T>G	NP_787046.1:n.1881+2T>G