Canonical Allele Identifier: CA408593169

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31395669A>C (hg19) ; chr20:g.32807863A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807863A>C , CM000682.2:g.32807863A>C	GRCh38
NC_000020.10:g.31395669A>C , CM000682.1:g.31395669A>C	GRCh37
NC_000020.9:g.30859330A>C	NCBI36
NG_007290.1:g.50479A>C , LRG_56:g.50479A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696231.1:c.*1473A>C	ENSP00000512497.1:n.*1473A>C
ENST00000696232.1:c.2333A>C	ENSP00000512498.1:p.His778Pro
ENST00000696233.1:c.*1076A>C	ENSP00000512499.1:n.*1076A>C
ENST00000696238.1:c.*1265A>C	ENSP00000512502.1:n.*1265A>C
ENST00000696239.1:c.2303A>C	ENSP00000512503.1:p.His768Pro
ENST00000696245.1:n.547A>C
ENST00000201963.3:c.2498A>C	ENSP00000201963.3:p.His833Pro
ENST00000328111.6:c.2522A>C MANE Select	ENSP00000328547.2:p.His841Pro
ENST00000348286.6:c.2273A>C	ENSP00000337764.2:p.His758Pro
ENST00000353855.6:c.2462A>C	ENSP00000313397.4:p.His821Pro
ENST00000443239.7:c.2147A>C	ENSP00000403169.2:p.His716Pro
ENST00000456297.6:c.2045A>C	ENSP00000412305.1:p.His682Pro
NM_001207055.1:c.2147A>C	NP_001193984.1:p.His716Pro
NM_001207056.1:c.2045A>C	NP_001193985.1:p.His682Pro
NM_006892.3:c.2522A>C , LRG_56t1:c.2522A>C	NP_008823.1:p.His841Pro
NM_175848.1:c.2462A>C	NP_787044.1:p.His821Pro
NM_175849.1:c.2273A>C	NP_787045.1:p.His758Pro
NM_175850.2:c.2498A>C	NP_787046.1:p.His833Pro
XM_011528653.1:c.2309A>C	XP_011526955.1:p.His770Pro
XM_011528654.1:c.2183A>C	XP_011526956.1:p.His728Pro
XR_936511.1:n.2300A>C
XM_011528653.2:c.2309A>C	XP_011526955.1:p.His770Pro
XM_011528654.2:c.2183A>C	XP_011526956.1:p.His728Pro
XR_936511.2:n.2311A>C
NM_001207055.2:c.2147A>C	NP_001193984.1:p.His716Pro
NM_001207056.2:c.2045A>C	NP_001193985.1:p.His682Pro
NM_006892.4:c.2522A>C MANE Select	NP_008823.1:p.His841Pro
NM_175848.2:c.2462A>C	NP_787044.1:p.His821Pro
NM_175849.2:c.2273A>C	NP_787045.1:p.His758Pro
NM_175850.3:c.2498A>C	NP_787046.1:p.His833Pro