Canonical Allele Identifier: CA510212109

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31393202A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32805396A>C , CM000682.2:g.32805396A>C	GRCh38
NC_000020.10:g.31393202A>C , CM000682.1:g.31393202A>C	GRCh37
NC_000020.9:g.30856863A>C	NCBI36
NG_007290.1:g.48012A>C , LRG_56:g.48012A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1241A>C	ENSP00000512497.1:n.*1241A>C
ENST00000696232.1:c.2232-2366A>C	ENSP00000512498.1:n.2232-2366A>C
ENST00000696233.1:c.*975-2366A>C	ENSP00000512499.1:n.*975-2366A>C
ENST00000696238.1:c.*1033A>C	ENSP00000512502.1:n.*1033A>C
ENST00000696239.1:c.2071A>C	ENSP00000512503.1:p.Arg691=
ENST00000696245.1:n.327-813A>C
ENST00000201963.3:c.2266A>C	ENSP00000201963.3:p.Arg756=
ENST00000328111.6:c.2290A>C MANE Select	ENSP00000328547.2:p.Arg764=
ENST00000348286.6:c.2172-2366A>C	ENSP00000337764.2:n.2172-2366A>C
ENST00000353855.6:c.2230A>C	ENSP00000313397.4:p.Arg744=
ENST00000443239.7:c.2046-2366A>C	ENSP00000403169.2:n.2046-2366A>C
ENST00000456297.6:c.1944-2366A>C	ENSP00000412305.1:n.1944-2366A>C
NM_001207055.1:c.2046-2366A>C	NP_001193984.1:n.2046-2366A>C
NM_001207056.1:c.1944-2366A>C	NP_001193985.1:n.1944-2366A>C
NM_006892.3:c.2290A>C , LRG_56t1:c.2290A>C	NP_008823.1:p.Arg764=
NM_175848.1:c.2230A>C	NP_787044.1:p.Arg744=
NM_175849.1:c.2172-2366A>C	NP_787045.1:n.2172-2366A>C
NM_175850.2:c.2266A>C	NP_787046.1:p.Arg756=
XM_011528653.1:c.2208-2366A>C	XP_011526955.1:n.2208-2366A>C
XM_011528654.1:c.2082-2366A>C	XP_011526956.1:n.2082-2366A>C
XR_936510.1:n.2257A>C
XR_936511.1:n.2199-2366A>C
XR_936512.1:n.2132A>C
XM_011528653.2:c.2208-2366A>C	XP_011526955.1:n.2208-2366A>C
XM_011528654.2:c.2082-2366A>C	XP_011526956.1:n.2082-2366A>C
XR_936510.2:n.2268A>C
XR_936511.2:n.2210-2366A>C
XR_936512.2:n.2144A>C
NM_001207055.2:c.2046-2366A>C	NP_001193984.1:n.2046-2366A>C
NM_001207056.2:c.1944-2366A>C	NP_001193985.1:n.1944-2366A>C
NM_006892.4:c.2290A>C MANE Select	NP_008823.1:p.Arg764=
NM_175848.2:c.2230A>C	NP_787044.1:p.Arg744=
NM_175849.2:c.2172-2366A>C	NP_787045.1:n.2172-2366A>C
NM_175850.3:c.2266A>C	NP_787046.1:p.Arg756=