Canonical Allele Identifier: CA408593235

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31395687A>T (hg19) ; chr20:g.32807881A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807881A>T , CM000682.2:g.32807881A>T	GRCh38
NC_000020.10:g.31395687A>T , CM000682.1:g.31395687A>T	GRCh37
NC_000020.9:g.30859348A>T	NCBI36
NG_007290.1:g.50497A>T , LRG_56:g.50497A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1491A>T	ENSP00000512497.1:n.*1491A>T
ENST00000696232.1:c.2351A>T	ENSP00000512498.1:p.Lys784Met
ENST00000696233.1:c.*1094A>T	ENSP00000512499.1:n.*1094A>T
ENST00000696238.1:c.*1283A>T	ENSP00000512502.1:n.*1283A>T
ENST00000696239.1:c.2321A>T	ENSP00000512503.1:p.Lys774Met
ENST00000696245.1:n.565A>T
ENST00000201963.3:c.2516A>T	ENSP00000201963.3:p.Lys839Met
ENST00000328111.6:c.2540A>T MANE Select	ENSP00000328547.2:p.Lys847Met
ENST00000348286.6:c.2291A>T	ENSP00000337764.2:p.Lys764Met
ENST00000353855.6:c.2480A>T	ENSP00000313397.4:p.Lys827Met
ENST00000443239.7:c.2165A>T	ENSP00000403169.2:p.Lys722Met
ENST00000456297.6:c.2063A>T	ENSP00000412305.1:p.Lys688Met
NM_001207055.1:c.2165A>T	NP_001193984.1:p.Lys722Met
NM_001207056.1:c.2063A>T	NP_001193985.1:p.Lys688Met
NM_006892.3:c.2540A>T , LRG_56t1:c.2540A>T	NP_008823.1:p.Lys847Met
NM_175848.1:c.2480A>T	NP_787044.1:p.Lys827Met
NM_175849.1:c.2291A>T	NP_787045.1:p.Lys764Met
NM_175850.2:c.2516A>T	NP_787046.1:p.Lys839Met
XM_011528653.1:c.2327A>T	XP_011526955.1:p.Lys776Met
XM_011528654.1:c.2201A>T	XP_011526956.1:p.Lys734Met
XR_936511.1:n.2318A>T
XM_011528653.2:c.2327A>T	XP_011526955.1:p.Lys776Met
XM_011528654.2:c.2201A>T	XP_011526956.1:p.Lys734Met
XR_936511.2:n.2329A>T
NM_001207055.2:c.2165A>T	NP_001193984.1:p.Lys722Met
NM_001207056.2:c.2063A>T	NP_001193985.1:p.Lys688Met
NM_006892.4:c.2540A>T MANE Select	NP_008823.1:p.Lys847Met
NM_175848.2:c.2480A>T	NP_787044.1:p.Lys827Met
NM_175849.2:c.2291A>T	NP_787045.1:p.Lys764Met
NM_175850.3:c.2516A>T	NP_787046.1:p.Lys839Met