Canonical Allele Identifier: CA408588390

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31388020T>A (hg19) ; chr20:g.32800214T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32800214T>A , CM000682.2:g.32800214T>A	GRCh38
NC_000020.10:g.31388020T>A , CM000682.1:g.31388020T>A	GRCh37
NC_000020.9:g.30851681T>A	NCBI36
NG_007290.1:g.42830T>A , LRG_56:g.42830T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*772T>A	ENSP00000512497.1:n.*772T>A
ENST00000696232.1:c.1821T>A	ENSP00000512498.1:p.Cys607Ter
ENST00000696233.1:c.*564T>A	ENSP00000512499.1:n.*564T>A
ENST00000696235.1:c.*469T>A	ENSP00000512500.1:n.*469T>A
ENST00000696238.1:c.*564T>A	ENSP00000512502.1:n.*564T>A
ENST00000696239.1:c.1602T>A	ENSP00000512503.1:p.Cys534Ter
ENST00000201963.3:c.1797T>A	ENSP00000201963.3:p.Cys599Ter
ENST00000328111.6:c.1821T>A MANE Select	ENSP00000328547.2:p.Cys607Ter
ENST00000348286.6:c.1761T>A	ENSP00000337764.2:p.Cys587Ter
ENST00000353855.6:c.1761T>A	ENSP00000313397.4:p.Cys587Ter
ENST00000443239.7:c.1635T>A	ENSP00000403169.2:p.Cys545Ter
ENST00000456297.6:c.1533T>A	ENSP00000412305.1:p.Cys511Ter
NM_001207055.1:c.1635T>A	NP_001193984.1:p.Cys545Ter
NM_001207056.1:c.1533T>A	NP_001193985.1:p.Cys511Ter
NM_006892.3:c.1821T>A , LRG_56t1:c.1821T>A	NP_008823.1:p.Cys607Ter
NM_175848.1:c.1761T>A	NP_787044.1:p.Cys587Ter
NM_175849.1:c.1761T>A	NP_787045.1:p.Cys587Ter
NM_175850.2:c.1797T>A	NP_787046.1:p.Cys599Ter
XM_011528653.1:c.1797T>A	XP_011526955.1:p.Cys599Ter
XM_011528654.1:c.1671T>A	XP_011526956.1:p.Cys557Ter
XR_936510.1:n.1788T>A
XR_936511.1:n.1788T>A
XR_936512.1:n.1663T>A
XM_011528653.2:c.1797T>A	XP_011526955.1:p.Cys599Ter
XM_011528654.2:c.1671T>A	XP_011526956.1:p.Cys557Ter
XR_936510.2:n.1799T>A
XR_936511.2:n.1799T>A
XR_936512.2:n.1675T>A
NM_001207055.2:c.1635T>A	NP_001193984.1:p.Cys545Ter
NM_001207056.2:c.1533T>A	NP_001193985.1:p.Cys511Ter
NM_006892.4:c.1821T>A MANE Select	NP_008823.1:p.Cys607Ter
NM_175848.2:c.1761T>A	NP_787044.1:p.Cys587Ter
NM_175849.2:c.1761T>A	NP_787045.1:p.Cys587Ter
NM_175850.3:c.1797T>A	NP_787046.1:p.Cys599Ter