Canonical Allele Identifier: CA408593162

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31395668C>T (hg19) ; chr20:g.32807862C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807862C>T , CM000682.2:g.32807862C>T	GRCh38
NC_000020.10:g.31395668C>T , CM000682.1:g.31395668C>T	GRCh37
NC_000020.9:g.30859329C>T	NCBI36
NG_007290.1:g.50478C>T , LRG_56:g.50478C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696231.1:c.*1472C>T	ENSP00000512497.1:n.*1472C>T
ENST00000696232.1:c.2332C>T	ENSP00000512498.1:p.His778Tyr
ENST00000696233.1:c.*1075C>T	ENSP00000512499.1:n.*1075C>T
ENST00000696238.1:c.*1264C>T	ENSP00000512502.1:n.*1264C>T
ENST00000696239.1:c.2302C>T	ENSP00000512503.1:p.His768Tyr
ENST00000696245.1:n.546C>T
ENST00000201963.3:c.2497C>T	ENSP00000201963.3:p.His833Tyr
ENST00000328111.6:c.2521C>T MANE Select	ENSP00000328547.2:p.His841Tyr
ENST00000348286.6:c.2272C>T	ENSP00000337764.2:p.His758Tyr
ENST00000353855.6:c.2461C>T	ENSP00000313397.4:p.His821Tyr
ENST00000443239.7:c.2146C>T	ENSP00000403169.2:p.His716Tyr
ENST00000456297.6:c.2044C>T	ENSP00000412305.1:p.His682Tyr
NM_001207055.1:c.2146C>T	NP_001193984.1:p.His716Tyr
NM_001207056.1:c.2044C>T	NP_001193985.1:p.His682Tyr
NM_006892.3:c.2521C>T , LRG_56t1:c.2521C>T	NP_008823.1:p.His841Tyr
NM_175848.1:c.2461C>T	NP_787044.1:p.His821Tyr
NM_175849.1:c.2272C>T	NP_787045.1:p.His758Tyr
NM_175850.2:c.2497C>T	NP_787046.1:p.His833Tyr
XM_011528653.1:c.2308C>T	XP_011526955.1:p.His770Tyr
XM_011528654.1:c.2182C>T	XP_011526956.1:p.His728Tyr
XR_936511.1:n.2299C>T
XM_011528653.2:c.2308C>T	XP_011526955.1:p.His770Tyr
XM_011528654.2:c.2182C>T	XP_011526956.1:p.His728Tyr
XR_936511.2:n.2310C>T
NM_001207055.2:c.2146C>T	NP_001193984.1:p.His716Tyr
NM_001207056.2:c.2044C>T	NP_001193985.1:p.His682Tyr
NM_006892.4:c.2521C>T MANE Select	NP_008823.1:p.His841Tyr
NM_175848.2:c.2461C>T	NP_787044.1:p.His821Tyr
NM_175849.2:c.2272C>T	NP_787045.1:p.His758Tyr
NM_175850.3:c.2497C>T	NP_787046.1:p.His833Tyr