Canonical Allele Identifier: CA510214599

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31395682T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807876T>A , CM000682.2:g.32807876T>A	GRCh38
NC_000020.10:g.31395682T>A , CM000682.1:g.31395682T>A	GRCh37
NC_000020.9:g.30859343T>A	NCBI36
NG_007290.1:g.50492T>A , LRG_56:g.50492T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1486T>A	ENSP00000512497.1:n.*1486T>A
ENST00000696232.1:c.2346T>A	ENSP00000512498.1:p.Pro782=
ENST00000696233.1:c.*1089T>A	ENSP00000512499.1:n.*1089T>A
ENST00000696238.1:c.*1278T>A	ENSP00000512502.1:n.*1278T>A
ENST00000696239.1:c.2316T>A	ENSP00000512503.1:p.Pro772=
ENST00000696245.1:n.560T>A
ENST00000201963.3:c.2511T>A	ENSP00000201963.3:p.Pro837=
ENST00000328111.6:c.2535T>A MANE Select	ENSP00000328547.2:p.Pro845=
ENST00000348286.6:c.2286T>A	ENSP00000337764.2:p.Pro762=
ENST00000353855.6:c.2475T>A	ENSP00000313397.4:p.Pro825=
ENST00000443239.7:c.2160T>A	ENSP00000403169.2:p.Pro720=
ENST00000456297.6:c.2058T>A	ENSP00000412305.1:p.Pro686=
NM_001207055.1:c.2160T>A	NP_001193984.1:p.Pro720=
NM_001207056.1:c.2058T>A	NP_001193985.1:p.Pro686=
NM_006892.3:c.2535T>A , LRG_56t1:c.2535T>A	NP_008823.1:p.Pro845=
NM_175848.1:c.2475T>A	NP_787044.1:p.Pro825=
NM_175849.1:c.2286T>A	NP_787045.1:p.Pro762=
NM_175850.2:c.2511T>A	NP_787046.1:p.Pro837=
XM_011528653.1:c.2322T>A	XP_011526955.1:p.Pro774=
XM_011528654.1:c.2196T>A	XP_011526956.1:p.Pro732=
XR_936511.1:n.2313T>A
XM_011528653.2:c.2322T>A	XP_011526955.1:p.Pro774=
XM_011528654.2:c.2196T>A	XP_011526956.1:p.Pro732=
XR_936511.2:n.2324T>A
NM_001207055.2:c.2160T>A	NP_001193984.1:p.Pro720=
NM_001207056.2:c.2058T>A	NP_001193985.1:p.Pro686=
NM_006892.4:c.2535T>A MANE Select	NP_008823.1:p.Pro845=
NM_175848.2:c.2475T>A	NP_787044.1:p.Pro825=
NM_175849.2:c.2286T>A	NP_787045.1:p.Pro762=
NM_175850.3:c.2511T>A	NP_787046.1:p.Pro837=