Canonical Allele Identifier: CA510469086

Gene: DNMT3B

Linked Data

• gnomAD v4: 20-32787352-T-C
• MyVariant Identifiers: chr20:g.31375158T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32787352T>C , CM000682.2:g.32787352T>C	GRCh38
NC_000020.10:g.31375158T>C , CM000682.1:g.31375158T>C	GRCh37
NC_000020.9:g.30838819T>C	NCBI36
NG_007290.1:g.29968T>C , LRG_56:g.29968T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.555T>C	ENSP00000512497.1:p.Ser185=
ENST00000696232.1:c.555T>C	ENSP00000512498.1:p.Ser185=
ENST00000696233.1:c.555T>C	ENSP00000512499.1:p.Ser185=
ENST00000696234.1:n.539T>C
ENST00000696235.1:c.429T>C	ENSP00000512500.1:p.Ser143=
ENST00000696236.1:c.429T>C	ENSP00000512501.1:p.Ser143=
ENST00000696237.1:n.661T>C
ENST00000696238.1:c.555T>C	ENSP00000512502.1:p.Ser185=
ENST00000696239.1:c.555T>C	ENSP00000512503.1:p.Ser185=
ENST00000201963.3:c.591T>C	ENSP00000201963.3:p.Ser197=
ENST00000328111.6:c.555T>C MANE Select	ENSP00000328547.2:p.Ser185=
ENST00000348286.6:c.555T>C	ENSP00000337764.2:p.Ser185=
ENST00000353855.6:c.555T>C	ENSP00000313397.4:p.Ser185=
ENST00000443239.7:c.429T>C	ENSP00000403169.2:p.Ser143=
ENST00000456297.6:c.327T>C	ENSP00000412305.1:p.Ser109=
NM_001207055.1:c.429T>C	NP_001193984.1:p.Ser143=
NM_001207056.1:c.327T>C	NP_001193985.1:p.Ser109=
NM_006892.3:c.555T>C , LRG_56t1:c.555T>C	NP_008823.1:p.Ser185=
NM_175848.1:c.555T>C	NP_787044.1:p.Ser185=
NM_175849.1:c.555T>C	NP_787045.1:p.Ser185=
NM_175850.2:c.591T>C	NP_787046.1:p.Ser197=
XM_011528653.1:c.591T>C	XP_011526955.1:p.Ser197=
XM_011528654.1:c.465T>C	XP_011526956.1:p.Ser155=
XR_936510.1:n.727T>C
XR_936511.1:n.727T>C
XR_936512.1:n.602T>C
XM_011528653.2:c.591T>C	XP_011526955.1:p.Ser197=
XM_011528654.2:c.465T>C	XP_011526956.1:p.Ser155=
XR_936510.2:n.738T>C
XR_936511.2:n.738T>C
XR_936512.2:n.614T>C
NM_001207055.2:c.429T>C	NP_001193984.1:p.Ser143=
NM_001207056.2:c.327T>C	NP_001193985.1:p.Ser109=
NM_006892.4:c.555T>C MANE Select	NP_008823.1:p.Ser185=
NM_175848.2:c.555T>C	NP_787044.1:p.Ser185=
NM_175849.2:c.555T>C	NP_787045.1:p.Ser185=
NM_175850.3:c.591T>C	NP_787046.1:p.Ser197=