Canonical Allele Identifier: CA408588529

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31388086G>C (hg19) ; chr20:g.32800280G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32800280G>C , CM000682.2:g.32800280G>C	GRCh38
NC_000020.10:g.31388086G>C , CM000682.1:g.31388086G>C	GRCh37
NC_000020.9:g.30851747G>C	NCBI36
NG_007290.1:g.42896G>C , LRG_56:g.42896G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*838G>C	ENSP00000512497.1:n.*838G>C
ENST00000696232.1:c.1887G>C	ENSP00000512498.1:p.Arg629Ser
ENST00000696233.1:c.*630G>C	ENSP00000512499.1:n.*630G>C
ENST00000696235.1:c.*535G>C	ENSP00000512500.1:n.*535G>C
ENST00000696238.1:c.*630G>C	ENSP00000512502.1:n.*630G>C
ENST00000696239.1:c.1668G>C	ENSP00000512503.1:p.Arg556Ser
ENST00000201963.3:c.1863G>C	ENSP00000201963.3:p.Arg621Ser
ENST00000328111.6:c.1887G>C MANE Select	ENSP00000328547.2:p.Arg629Ser
ENST00000348286.6:c.1827G>C	ENSP00000337764.2:p.Arg609Ser
ENST00000353855.6:c.1827G>C	ENSP00000313397.4:p.Arg609Ser
ENST00000443239.7:c.1701G>C	ENSP00000403169.2:p.Arg567Ser
ENST00000456297.6:c.1599G>C	ENSP00000412305.1:p.Arg533Ser
NM_001207055.1:c.1701G>C	NP_001193984.1:p.Arg567Ser
NM_001207056.1:c.1599G>C	NP_001193985.1:p.Arg533Ser
NM_006892.3:c.1887G>C , LRG_56t1:c.1887G>C	NP_008823.1:p.Arg629Ser
NM_175848.1:c.1827G>C	NP_787044.1:p.Arg609Ser
NM_175849.1:c.1827G>C	NP_787045.1:p.Arg609Ser
NM_175850.2:c.1863G>C	NP_787046.1:p.Arg621Ser
XM_011528653.1:c.1863G>C	XP_011526955.1:p.Arg621Ser
XM_011528654.1:c.1737G>C	XP_011526956.1:p.Arg579Ser
XR_936510.1:n.1854G>C
XR_936511.1:n.1854G>C
XR_936512.1:n.1729G>C
XM_011528653.2:c.1863G>C	XP_011526955.1:p.Arg621Ser
XM_011528654.2:c.1737G>C	XP_011526956.1:p.Arg579Ser
XR_936510.2:n.1865G>C
XR_936511.2:n.1865G>C
XR_936512.2:n.1741G>C
NM_001207055.2:c.1701G>C	NP_001193984.1:p.Arg567Ser
NM_001207056.2:c.1599G>C	NP_001193985.1:p.Arg533Ser
NM_006892.4:c.1887G>C MANE Select	NP_008823.1:p.Arg629Ser
NM_175848.2:c.1827G>C	NP_787044.1:p.Arg609Ser
NM_175849.2:c.1827G>C	NP_787045.1:p.Arg609Ser
NM_175850.3:c.1863G>C	NP_787046.1:p.Arg621Ser