Canonical Allele Identifier: CA510210619

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31388014A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32800208A>G , CM000682.2:g.32800208A>G	GRCh38
NC_000020.10:g.31388014A>G , CM000682.1:g.31388014A>G	GRCh37
NC_000020.9:g.30851675A>G	NCBI36
NG_007290.1:g.42824A>G , LRG_56:g.42824A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*766A>G	ENSP00000512497.1:n.*766A>G
ENST00000696232.1:c.1815A>G	ENSP00000512498.1:p.Glu605=
ENST00000696233.1:c.*558A>G	ENSP00000512499.1:n.*558A>G
ENST00000696235.1:c.*463A>G	ENSP00000512500.1:n.*463A>G
ENST00000696238.1:c.*558A>G	ENSP00000512502.1:n.*558A>G
ENST00000696239.1:c.1596A>G	ENSP00000512503.1:p.Glu532=
ENST00000201963.3:c.1791A>G	ENSP00000201963.3:p.Glu597=
ENST00000328111.6:c.1815A>G MANE Select	ENSP00000328547.2:p.Glu605=
ENST00000348286.6:c.1755A>G	ENSP00000337764.2:p.Glu585=
ENST00000353855.6:c.1755A>G	ENSP00000313397.4:p.Glu585=
ENST00000443239.7:c.1629A>G	ENSP00000403169.2:p.Glu543=
ENST00000456297.6:c.1527A>G	ENSP00000412305.1:p.Glu509=
NM_001207055.1:c.1629A>G	NP_001193984.1:p.Glu543=
NM_001207056.1:c.1527A>G	NP_001193985.1:p.Glu509=
NM_006892.3:c.1815A>G , LRG_56t1:c.1815A>G	NP_008823.1:p.Glu605=
NM_175848.1:c.1755A>G	NP_787044.1:p.Glu585=
NM_175849.1:c.1755A>G	NP_787045.1:p.Glu585=
NM_175850.2:c.1791A>G	NP_787046.1:p.Glu597=
XM_011528653.1:c.1791A>G	XP_011526955.1:p.Glu597=
XM_011528654.1:c.1665A>G	XP_011526956.1:p.Glu555=
XR_936510.1:n.1782A>G
XR_936511.1:n.1782A>G
XR_936512.1:n.1657A>G
XM_011528653.2:c.1791A>G	XP_011526955.1:p.Glu597=
XM_011528654.2:c.1665A>G	XP_011526956.1:p.Glu555=
XR_936510.2:n.1793A>G
XR_936511.2:n.1793A>G
XR_936512.2:n.1669A>G
NM_001207055.2:c.1629A>G	NP_001193984.1:p.Glu543=
NM_001207056.2:c.1527A>G	NP_001193985.1:p.Glu509=
NM_006892.4:c.1815A>G MANE Select	NP_008823.1:p.Glu605=
NM_175848.2:c.1755A>G	NP_787044.1:p.Glu585=
NM_175849.2:c.1755A>G	NP_787045.1:p.Glu585=
NM_175850.3:c.1791A>G	NP_787046.1:p.Glu597=