Canonical Allele Identifier: CA313185422

Gene: DNMT3B

Linked Data

• dbSNP Id: rs386813737

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32787579_32787580delinsTG , CM000682.2:g.32787579_32787580delinsTG	GRCh38
NC_000020.10:g.31375385_31375386delinsTG , CM000682.1:g.31375385_31375386delinsTG	GRCh37
NC_000020.9:g.30839046_30839047delinsTG	NCBI36
NG_007290.1:g.30195_30196delinsTG , LRG_56:g.30195_30196delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.654+128_654+129delinsTG	ENSP00000512497.1:n.654+128_654+129delinsTG
ENST00000696232.1:c.654+128_654+129delinsTG	ENSP00000512498.1:n.654+128_654+129delinsTG
ENST00000696233.1:c.654+128_654+129delinsTG	ENSP00000512499.1:n.654+128_654+129delinsTG
ENST00000696234.1:n.638+128_638+129delinsTG
ENST00000696235.1:c.528+128_528+129delinsTG	ENSP00000512500.1:n.528+128_528+129delinsTG
ENST00000696236.1:c.528+128_528+129delinsTG	ENSP00000512501.1:n.528+128_528+129delinsTG
ENST00000696238.1:c.654+128_654+129delinsTG	ENSP00000512502.1:n.654+128_654+129delinsTG
ENST00000696239.1:c.654+128_654+129delinsTG	ENSP00000512503.1:n.654+128_654+129delinsTG
ENST00000201963.3:c.690+128_690+129delinsTG	ENSP00000201963.3:n.690+128_690+129delinsTG
ENST00000328111.6:c.654+128_654+129delinsTG MANE Select	ENSP00000328547.2:n.654+128_654+129delinsTG
ENST00000348286.6:c.654+128_654+129delinsTG	ENSP00000337764.2:n.654+128_654+129delinsTG
ENST00000353855.6:c.654+128_654+129delinsTG	ENSP00000313397.4:n.654+128_654+129delinsTG
ENST00000443239.7:c.528+128_528+129delinsTG	ENSP00000403169.2:n.528+128_528+129delinsTG
ENST00000456297.6:c.426+128_426+129delinsTG	ENSP00000412305.1:n.426+128_426+129delinsTG
NM_001207055.1:c.528+128_528+129delinsTG	NP_001193984.1:n.528+128_528+129delinsTG
NM_001207056.1:c.426+128_426+129delinsTG	NP_001193985.1:n.426+128_426+129delinsTG
NM_006892.3:c.654+128_654+129delinsTG , LRG_56t1:c.654+128_654+129delinsTG	NP_008823.1:n.654+128_654+129delinsTG
NM_175848.1:c.654+128_654+129delinsTG	NP_787044.1:n.654+128_654+129delinsTG
NM_175849.1:c.654+128_654+129delinsTG	NP_787045.1:n.654+128_654+129delinsTG
NM_175850.2:c.690+128_690+129delinsTG	NP_787046.1:n.690+128_690+129delinsTG
XM_011528653.1:c.690+128_690+129delinsTG	XP_011526955.1:n.690+128_690+129delinsTG
XM_011528654.1:c.564+128_564+129delinsTG	XP_011526956.1:n.564+128_564+129delinsTG
XR_936510.1:n.826+128_826+129delinsTG
XR_936511.1:n.826+128_826+129delinsTG
XR_936512.1:n.701+128_701+129delinsTG
XM_011528653.2:c.690+128_690+129delinsTG	XP_011526955.1:n.690+128_690+129delinsTG
XM_011528654.2:c.564+128_564+129delinsTG	XP_011526956.1:n.564+128_564+129delinsTG
XR_936510.2:n.837+128_837+129delinsTG
XR_936511.2:n.837+128_837+129delinsTG
XR_936512.2:n.713+128_713+129delinsTG
NM_001207055.2:c.528+128_528+129delinsTG	NP_001193984.1:n.528+128_528+129delinsTG
NM_001207056.2:c.426+128_426+129delinsTG	NP_001193985.1:n.426+128_426+129delinsTG
NM_006892.4:c.654+128_654+129delinsTG MANE Select	NP_008823.1:n.654+128_654+129delinsTG
NM_175848.2:c.654+128_654+129delinsTG	NP_787044.1:n.654+128_654+129delinsTG
NM_175849.2:c.654+128_654+129delinsTG	NP_787045.1:n.654+128_654+129delinsTG
NM_175850.3:c.690+128_690+129delinsTG	NP_787046.1:n.690+128_690+129delinsTG