Canonical Allele Identifier: CA408593192

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31395674T>G (hg19) ; chr20:g.32807868T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807868T>G , CM000682.2:g.32807868T>G	GRCh38
NC_000020.10:g.31395674T>G , CM000682.1:g.31395674T>G	GRCh37
NC_000020.9:g.30859335T>G	NCBI36
NG_007290.1:g.50484T>G , LRG_56:g.50484T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1478T>G	ENSP00000512497.1:n.*1478T>G
ENST00000696232.1:c.2338T>G	ENSP00000512498.1:p.Phe780Val
ENST00000696233.1:c.*1081T>G	ENSP00000512499.1:n.*1081T>G
ENST00000696238.1:c.*1270T>G	ENSP00000512502.1:n.*1270T>G
ENST00000696239.1:c.2308T>G	ENSP00000512503.1:p.Phe770Val
ENST00000696245.1:n.552T>G
ENST00000201963.3:c.2503T>G	ENSP00000201963.3:p.Phe835Val
ENST00000328111.6:c.2527T>G MANE Select	ENSP00000328547.2:p.Phe843Val
ENST00000348286.6:c.2278T>G	ENSP00000337764.2:p.Phe760Val
ENST00000353855.6:c.2467T>G	ENSP00000313397.4:p.Phe823Val
ENST00000443239.7:c.2152T>G	ENSP00000403169.2:p.Phe718Val
ENST00000456297.6:c.2050T>G	ENSP00000412305.1:p.Phe684Val
NM_001207055.1:c.2152T>G	NP_001193984.1:p.Phe718Val
NM_001207056.1:c.2050T>G	NP_001193985.1:p.Phe684Val
NM_006892.3:c.2527T>G , LRG_56t1:c.2527T>G	NP_008823.1:p.Phe843Val
NM_175848.1:c.2467T>G	NP_787044.1:p.Phe823Val
NM_175849.1:c.2278T>G	NP_787045.1:p.Phe760Val
NM_175850.2:c.2503T>G	NP_787046.1:p.Phe835Val
XM_011528653.1:c.2314T>G	XP_011526955.1:p.Phe772Val
XM_011528654.1:c.2188T>G	XP_011526956.1:p.Phe730Val
XR_936511.1:n.2305T>G
XM_011528653.2:c.2314T>G	XP_011526955.1:p.Phe772Val
XM_011528654.2:c.2188T>G	XP_011526956.1:p.Phe730Val
XR_936511.2:n.2316T>G
NM_001207055.2:c.2152T>G	NP_001193984.1:p.Phe718Val
NM_001207056.2:c.2050T>G	NP_001193985.1:p.Phe684Val
NM_006892.4:c.2527T>G MANE Select	NP_008823.1:p.Phe843Val
NM_175848.2:c.2467T>G	NP_787044.1:p.Phe823Val
NM_175849.2:c.2278T>G	NP_787045.1:p.Phe760Val
NM_175850.3:c.2503T>G	NP_787046.1:p.Phe835Val