Canonical Allele Identifier: CA510212116

Gene: DNMT3B

Linked Data

• dbSNP Id: rs759448571
• gnomAD v2: 20-31393204-G-A
• gnomAD v4: 20-32805398-G-A
• MyVariant Identifiers: chr20:g.31393204G>A (hg19) ; chr20:g.32805398G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32805398G>A , CM000682.2:g.32805398G>A	GRCh38
NC_000020.10:g.31393204G>A , CM000682.1:g.31393204G>A	GRCh37
NC_000020.9:g.30856865G>A	NCBI36
NG_007290.1:g.48014G>A , LRG_56:g.48014G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1243G>A	ENSP00000512497.1:n.*1243G>A
ENST00000696232.1:c.2232-2364G>A	ENSP00000512498.1:n.2232-2364G>A
ENST00000696233.1:c.*975-2364G>A	ENSP00000512499.1:n.*975-2364G>A
ENST00000696238.1:c.*1035G>A	ENSP00000512502.1:n.*1035G>A
ENST00000696239.1:c.2073G>A	ENSP00000512503.1:p.Arg691=
ENST00000696245.1:n.327-811G>A
ENST00000201963.3:c.2268G>A	ENSP00000201963.3:p.Arg756=
ENST00000328111.6:c.2292G>A MANE Select	ENSP00000328547.2:p.Arg764=
ENST00000348286.6:c.2172-2364G>A	ENSP00000337764.2:n.2172-2364G>A
ENST00000353855.6:c.2232G>A	ENSP00000313397.4:p.Arg744=
ENST00000443239.7:c.2046-2364G>A	ENSP00000403169.2:n.2046-2364G>A
ENST00000456297.6:c.1944-2364G>A	ENSP00000412305.1:n.1944-2364G>A
NM_001207055.1:c.2046-2364G>A	NP_001193984.1:n.2046-2364G>A
NM_001207056.1:c.1944-2364G>A	NP_001193985.1:n.1944-2364G>A
NM_006892.3:c.2292G>A , LRG_56t1:c.2292G>A	NP_008823.1:p.Arg764=
NM_175848.1:c.2232G>A	NP_787044.1:p.Arg744=
NM_175849.1:c.2172-2364G>A	NP_787045.1:n.2172-2364G>A
NM_175850.2:c.2268G>A	NP_787046.1:p.Arg756=
XM_011528653.1:c.2208-2364G>A	XP_011526955.1:n.2208-2364G>A
XM_011528654.1:c.2082-2364G>A	XP_011526956.1:n.2082-2364G>A
XR_936510.1:n.2259G>A
XR_936511.1:n.2199-2364G>A
XR_936512.1:n.2134G>A
XM_011528653.2:c.2208-2364G>A	XP_011526955.1:n.2208-2364G>A
XM_011528654.2:c.2082-2364G>A	XP_011526956.1:n.2082-2364G>A
XR_936510.2:n.2270G>A
XR_936511.2:n.2210-2364G>A
XR_936512.2:n.2146G>A
NM_001207055.2:c.2046-2364G>A	NP_001193984.1:n.2046-2364G>A
NM_001207056.2:c.1944-2364G>A	NP_001193985.1:n.1944-2364G>A
NM_006892.4:c.2292G>A MANE Select	NP_008823.1:p.Arg764=
NM_175848.2:c.2232G>A	NP_787044.1:p.Arg744=
NM_175849.2:c.2172-2364G>A	NP_787045.1:n.2172-2364G>A
NM_175850.3:c.2268G>A	NP_787046.1:p.Arg756=