Canonical Allele Identifier: CA510210660

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31388074G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32800268G>A , CM000682.2:g.32800268G>A	GRCh38
NC_000020.10:g.31388074G>A , CM000682.1:g.31388074G>A	GRCh37
NC_000020.9:g.30851735G>A	NCBI36
NG_007290.1:g.42884G>A , LRG_56:g.42884G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*826G>A	ENSP00000512497.1:n.*826G>A
ENST00000696232.1:c.1875G>A	ENSP00000512498.1:p.Val625=
ENST00000696233.1:c.*618G>A	ENSP00000512499.1:n.*618G>A
ENST00000696235.1:c.*523G>A	ENSP00000512500.1:n.*523G>A
ENST00000696238.1:c.*618G>A	ENSP00000512502.1:n.*618G>A
ENST00000696239.1:c.1656G>A	ENSP00000512503.1:p.Val552=
ENST00000201963.3:c.1851G>A	ENSP00000201963.3:p.Val617=
ENST00000328111.6:c.1875G>A MANE Select	ENSP00000328547.2:p.Val625=
ENST00000348286.6:c.1815G>A	ENSP00000337764.2:p.Val605=
ENST00000353855.6:c.1815G>A	ENSP00000313397.4:p.Val605=
ENST00000443239.7:c.1689G>A	ENSP00000403169.2:p.Val563=
ENST00000456297.6:c.1587G>A	ENSP00000412305.1:p.Val529=
NM_001207055.1:c.1689G>A	NP_001193984.1:p.Val563=
NM_001207056.1:c.1587G>A	NP_001193985.1:p.Val529=
NM_006892.3:c.1875G>A , LRG_56t1:c.1875G>A	NP_008823.1:p.Val625=
NM_175848.1:c.1815G>A	NP_787044.1:p.Val605=
NM_175849.1:c.1815G>A	NP_787045.1:p.Val605=
NM_175850.2:c.1851G>A	NP_787046.1:p.Val617=
XM_011528653.1:c.1851G>A	XP_011526955.1:p.Val617=
XM_011528654.1:c.1725G>A	XP_011526956.1:p.Val575=
XR_936510.1:n.1842G>A
XR_936511.1:n.1842G>A
XR_936512.1:n.1717G>A
XM_011528653.2:c.1851G>A	XP_011526955.1:p.Val617=
XM_011528654.2:c.1725G>A	XP_011526956.1:p.Val575=
XR_936510.2:n.1853G>A
XR_936511.2:n.1853G>A
XR_936512.2:n.1729G>A
NM_001207055.2:c.1689G>A	NP_001193984.1:p.Val563=
NM_001207056.2:c.1587G>A	NP_001193985.1:p.Val529=
NM_006892.4:c.1875G>A MANE Select	NP_008823.1:p.Val625=
NM_175848.2:c.1815G>A	NP_787044.1:p.Val605=
NM_175849.2:c.1815G>A	NP_787045.1:p.Val605=
NM_175850.3:c.1851G>A	NP_787046.1:p.Val617=