Canonical Allele Identifier: CA510214293

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31395619T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807813T>C , CM000682.2:g.32807813T>C	GRCh38
NC_000020.10:g.31395619T>C , CM000682.1:g.31395619T>C	GRCh37
NC_000020.9:g.30859280T>C	NCBI36
NG_007290.1:g.50429T>C , LRG_56:g.50429T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1423T>C	ENSP00000512497.1:n.*1423T>C
ENST00000696232.1:c.2283T>C	ENSP00000512498.1:p.Gly761=
ENST00000696233.1:c.*1026T>C	ENSP00000512499.1:n.*1026T>C
ENST00000696238.1:c.*1215T>C	ENSP00000512502.1:n.*1215T>C
ENST00000696239.1:c.2253T>C	ENSP00000512503.1:p.Gly751=
ENST00000696245.1:n.497T>C
ENST00000201963.3:c.2448T>C	ENSP00000201963.3:p.Gly816=
ENST00000328111.6:c.2472T>C MANE Select	ENSP00000328547.2:p.Gly824=
ENST00000348286.6:c.2223T>C	ENSP00000337764.2:p.Gly741=
ENST00000353855.6:c.2412T>C	ENSP00000313397.4:p.Gly804=
ENST00000443239.7:c.2097T>C	ENSP00000403169.2:p.Gly699=
ENST00000456297.6:c.1995T>C	ENSP00000412305.1:p.Gly665=
NM_001207055.1:c.2097T>C	NP_001193984.1:p.Gly699=
NM_001207056.1:c.1995T>C	NP_001193985.1:p.Gly665=
NM_006892.3:c.2472T>C , LRG_56t1:c.2472T>C	NP_008823.1:p.Gly824=
NM_175848.1:c.2412T>C	NP_787044.1:p.Gly804=
NM_175849.1:c.2223T>C	NP_787045.1:p.Gly741=
NM_175850.2:c.2448T>C	NP_787046.1:p.Gly816=
XM_011528653.1:c.2259T>C	XP_011526955.1:p.Gly753=
XM_011528654.1:c.2133T>C	XP_011526956.1:p.Gly711=
XR_936511.1:n.2250T>C
XM_011528653.2:c.2259T>C	XP_011526955.1:p.Gly753=
XM_011528654.2:c.2133T>C	XP_011526956.1:p.Gly711=
XR_936511.2:n.2261T>C
NM_001207055.2:c.2097T>C	NP_001193984.1:p.Gly699=
NM_001207056.2:c.1995T>C	NP_001193985.1:p.Gly665=
NM_006892.4:c.2472T>C MANE Select	NP_008823.1:p.Gly824=
NM_175848.2:c.2412T>C	NP_787044.1:p.Gly804=
NM_175849.2:c.2223T>C	NP_787045.1:p.Gly741=
NM_175850.3:c.2448T>C	NP_787046.1:p.Gly816=