Canonical Allele Identifier: CA408593097

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31395650A>C (hg19) ; chr20:g.32807844A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807844A>C , CM000682.2:g.32807844A>C	GRCh38
NC_000020.10:g.31395650A>C , CM000682.1:g.31395650A>C	GRCh37
NC_000020.9:g.30859311A>C	NCBI36
NG_007290.1:g.50460A>C , LRG_56:g.50460A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1454A>C	ENSP00000512497.1:n.*1454A>C
ENST00000696232.1:c.2314A>C	ENSP00000512498.1:p.Ser772Arg
ENST00000696233.1:c.*1057A>C	ENSP00000512499.1:n.*1057A>C
ENST00000696238.1:c.*1246A>C	ENSP00000512502.1:n.*1246A>C
ENST00000696239.1:c.2284A>C	ENSP00000512503.1:p.Ser762Arg
ENST00000696245.1:n.528A>C
ENST00000201963.3:c.2479A>C	ENSP00000201963.3:p.Ser827Arg
ENST00000328111.6:c.2503A>C MANE Select	ENSP00000328547.2:p.Ser835Arg
ENST00000348286.6:c.2254A>C	ENSP00000337764.2:p.Ser752Arg
ENST00000353855.6:c.2443A>C	ENSP00000313397.4:p.Ser815Arg
ENST00000443239.7:c.2128A>C	ENSP00000403169.2:p.Ser710Arg
ENST00000456297.6:c.2026A>C	ENSP00000412305.1:p.Ser676Arg
NM_001207055.1:c.2128A>C	NP_001193984.1:p.Ser710Arg
NM_001207056.1:c.2026A>C	NP_001193985.1:p.Ser676Arg
NM_006892.3:c.2503A>C , LRG_56t1:c.2503A>C	NP_008823.1:p.Ser835Arg
NM_175848.1:c.2443A>C	NP_787044.1:p.Ser815Arg
NM_175849.1:c.2254A>C	NP_787045.1:p.Ser752Arg
NM_175850.2:c.2479A>C	NP_787046.1:p.Ser827Arg
XM_011528653.1:c.2290A>C	XP_011526955.1:p.Ser764Arg
XM_011528654.1:c.2164A>C	XP_011526956.1:p.Ser722Arg
XR_936511.1:n.2281A>C
XM_011528653.2:c.2290A>C	XP_011526955.1:p.Ser764Arg
XM_011528654.2:c.2164A>C	XP_011526956.1:p.Ser722Arg
XR_936511.2:n.2292A>C
NM_001207055.2:c.2128A>C	NP_001193984.1:p.Ser710Arg
NM_001207056.2:c.2026A>C	NP_001193985.1:p.Ser676Arg
NM_006892.4:c.2503A>C MANE Select	NP_008823.1:p.Ser835Arg
NM_175848.2:c.2443A>C	NP_787044.1:p.Ser815Arg
NM_175849.2:c.2254A>C	NP_787045.1:p.Ser752Arg
NM_175850.3:c.2479A>C	NP_787046.1:p.Ser827Arg