Canonical Allele Identifier: CA510214590

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31395679C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807873C>A , CM000682.2:g.32807873C>A	GRCh38
NC_000020.10:g.31395679C>A , CM000682.1:g.31395679C>A	GRCh37
NC_000020.9:g.30859340C>A	NCBI36
NG_007290.1:g.50489C>A , LRG_56:g.50489C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1483C>A	ENSP00000512497.1:n.*1483C>A
ENST00000696232.1:c.2343C>A	ENSP00000512498.1:p.Ala781=
ENST00000696233.1:c.*1086C>A	ENSP00000512499.1:n.*1086C>A
ENST00000696238.1:c.*1275C>A	ENSP00000512502.1:n.*1275C>A
ENST00000696239.1:c.2313C>A	ENSP00000512503.1:p.Ala771=
ENST00000696245.1:n.557C>A
ENST00000201963.3:c.2508C>A	ENSP00000201963.3:p.Ala836=
ENST00000328111.6:c.2532C>A MANE Select	ENSP00000328547.2:p.Ala844=
ENST00000348286.6:c.2283C>A	ENSP00000337764.2:p.Ala761=
ENST00000353855.6:c.2472C>A	ENSP00000313397.4:p.Ala824=
ENST00000443239.7:c.2157C>A	ENSP00000403169.2:p.Ala719=
ENST00000456297.6:c.2055C>A	ENSP00000412305.1:p.Ala685=
NM_001207055.1:c.2157C>A	NP_001193984.1:p.Ala719=
NM_001207056.1:c.2055C>A	NP_001193985.1:p.Ala685=
NM_006892.3:c.2532C>A , LRG_56t1:c.2532C>A	NP_008823.1:p.Ala844=
NM_175848.1:c.2472C>A	NP_787044.1:p.Ala824=
NM_175849.1:c.2283C>A	NP_787045.1:p.Ala761=
NM_175850.2:c.2508C>A	NP_787046.1:p.Ala836=
XM_011528653.1:c.2319C>A	XP_011526955.1:p.Ala773=
XM_011528654.1:c.2193C>A	XP_011526956.1:p.Ala731=
XR_936511.1:n.2310C>A
XM_011528653.2:c.2319C>A	XP_011526955.1:p.Ala773=
XM_011528654.2:c.2193C>A	XP_011526956.1:p.Ala731=
XR_936511.2:n.2321C>A
NM_001207055.2:c.2157C>A	NP_001193984.1:p.Ala719=
NM_001207056.2:c.2055C>A	NP_001193985.1:p.Ala685=
NM_006892.4:c.2532C>A MANE Select	NP_008823.1:p.Ala844=
NM_175848.2:c.2472C>A	NP_787044.1:p.Ala824=
NM_175849.2:c.2283C>A	NP_787045.1:p.Ala761=
NM_175850.3:c.2508C>A	NP_787046.1:p.Ala836=