Canonical Allele Identifier: CA408593074

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31395642G>C (hg19) ; chr20:g.32807836G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807836G>C , CM000682.2:g.32807836G>C	GRCh38
NC_000020.10:g.31395642G>C , CM000682.1:g.31395642G>C	GRCh37
NC_000020.9:g.30859303G>C	NCBI36
NG_007290.1:g.50452G>C , LRG_56:g.50452G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1446G>C	ENSP00000512497.1:n.*1446G>C
ENST00000696232.1:c.2306G>C	ENSP00000512498.1:p.Arg769Thr
ENST00000696233.1:c.*1049G>C	ENSP00000512499.1:n.*1049G>C
ENST00000696238.1:c.*1238G>C	ENSP00000512502.1:n.*1238G>C
ENST00000696239.1:c.2276G>C	ENSP00000512503.1:p.Arg759Thr
ENST00000696245.1:n.520G>C
ENST00000201963.3:c.2471G>C	ENSP00000201963.3:p.Arg824Thr
ENST00000328111.6:c.2495G>C MANE Select	ENSP00000328547.2:p.Arg832Thr
ENST00000348286.6:c.2246G>C	ENSP00000337764.2:p.Arg749Thr
ENST00000353855.6:c.2435G>C	ENSP00000313397.4:p.Arg812Thr
ENST00000443239.7:c.2120G>C	ENSP00000403169.2:p.Arg707Thr
ENST00000456297.6:c.2018G>C	ENSP00000412305.1:p.Arg673Thr
NM_001207055.1:c.2120G>C	NP_001193984.1:p.Arg707Thr
NM_001207056.1:c.2018G>C	NP_001193985.1:p.Arg673Thr
NM_006892.3:c.2495G>C , LRG_56t1:c.2495G>C	NP_008823.1:p.Arg832Thr
NM_175848.1:c.2435G>C	NP_787044.1:p.Arg812Thr
NM_175849.1:c.2246G>C	NP_787045.1:p.Arg749Thr
NM_175850.2:c.2471G>C	NP_787046.1:p.Arg824Thr
XM_011528653.1:c.2282G>C	XP_011526955.1:p.Arg761Thr
XM_011528654.1:c.2156G>C	XP_011526956.1:p.Arg719Thr
XR_936511.1:n.2273G>C
XM_011528653.2:c.2282G>C	XP_011526955.1:p.Arg761Thr
XM_011528654.2:c.2156G>C	XP_011526956.1:p.Arg719Thr
XR_936511.2:n.2284G>C
NM_001207055.2:c.2120G>C	NP_001193984.1:p.Arg707Thr
NM_001207056.2:c.2018G>C	NP_001193985.1:p.Arg673Thr
NM_006892.4:c.2495G>C MANE Select	NP_008823.1:p.Arg832Thr
NM_175848.2:c.2435G>C	NP_787044.1:p.Arg812Thr
NM_175849.2:c.2246G>C	NP_787045.1:p.Arg749Thr
NM_175850.3:c.2471G>C	NP_787046.1:p.Arg824Thr