Canonical Allele Identifier: CA408586489

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31375075T>C (hg19) ; chr20:g.32787269T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32787269T>C , CM000682.2:g.32787269T>C	GRCh38
NC_000020.10:g.31375075T>C , CM000682.1:g.31375075T>C	GRCh37
NC_000020.9:g.30838736T>C	NCBI36
NG_007290.1:g.29885T>C , LRG_56:g.29885T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.472T>C	ENSP00000512497.1:p.Trp158Arg
ENST00000696232.1:c.472T>C	ENSP00000512498.1:p.Trp158Arg
ENST00000696233.1:c.472T>C	ENSP00000512499.1:p.Trp158Arg
ENST00000696234.1:n.456T>C
ENST00000696235.1:c.346T>C	ENSP00000512500.1:p.Trp116Arg
ENST00000696236.1:c.346T>C	ENSP00000512501.1:p.Trp116Arg
ENST00000696237.1:n.578T>C
ENST00000696238.1:c.472T>C	ENSP00000512502.1:p.Trp158Arg
ENST00000696239.1:c.472T>C	ENSP00000512503.1:p.Trp158Arg
ENST00000201963.3:c.508T>C	ENSP00000201963.3:p.Trp170Arg
ENST00000328111.6:c.472T>C MANE Select	ENSP00000328547.2:p.Trp158Arg
ENST00000348286.6:c.472T>C	ENSP00000337764.2:p.Trp158Arg
ENST00000353855.6:c.472T>C	ENSP00000313397.4:p.Trp158Arg
ENST00000443239.7:c.346T>C	ENSP00000403169.2:p.Trp116Arg
ENST00000456297.6:c.244T>C	ENSP00000412305.1:p.Trp82Arg
NM_001207055.1:c.346T>C	NP_001193984.1:p.Trp116Arg
NM_001207056.1:c.244T>C	NP_001193985.1:p.Trp82Arg
NM_006892.3:c.472T>C , LRG_56t1:c.472T>C	NP_008823.1:p.Trp158Arg
NM_175848.1:c.472T>C	NP_787044.1:p.Trp158Arg
NM_175849.1:c.472T>C	NP_787045.1:p.Trp158Arg
NM_175850.2:c.508T>C	NP_787046.1:p.Trp170Arg
XM_011528653.1:c.508T>C	XP_011526955.1:p.Trp170Arg
XM_011528654.1:c.382T>C	XP_011526956.1:p.Trp128Arg
XR_936510.1:n.644T>C
XR_936511.1:n.644T>C
XR_936512.1:n.519T>C
XM_011528653.2:c.508T>C	XP_011526955.1:p.Trp170Arg
XM_011528654.2:c.382T>C	XP_011526956.1:p.Trp128Arg
XR_936510.2:n.655T>C
XR_936511.2:n.655T>C
XR_936512.2:n.531T>C
NM_001207055.2:c.346T>C	NP_001193984.1:p.Trp116Arg
NM_001207056.2:c.244T>C	NP_001193985.1:p.Trp82Arg
NM_006892.4:c.472T>C MANE Select	NP_008823.1:p.Trp158Arg
NM_175848.2:c.472T>C	NP_787044.1:p.Trp158Arg
NM_175849.2:c.472T>C	NP_787045.1:p.Trp158Arg
NM_175850.3:c.508T>C	NP_787046.1:p.Trp170Arg