Canonical Allele Identifier: CA408593259

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31395693A>T (hg19) ; chr20:g.32807887A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807887A>T , CM000682.2:g.32807887A>T	GRCh38
NC_000020.10:g.31395693A>T , CM000682.1:g.31395693A>T	GRCh37
NC_000020.9:g.30859354A>T	NCBI36
NG_007290.1:g.50503A>T , LRG_56:g.50503A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1497A>T	ENSP00000512497.1:n.*1497A>T
ENST00000696232.1:c.2357A>T	ENSP00000512498.1:p.Tyr786Phe
ENST00000696233.1:c.*1100A>T	ENSP00000512499.1:n.*1100A>T
ENST00000696238.1:c.*1289A>T	ENSP00000512502.1:n.*1289A>T
ENST00000696239.1:c.2327A>T	ENSP00000512503.1:p.Tyr776Phe
ENST00000696245.1:n.571A>T
ENST00000201963.3:c.2522A>T	ENSP00000201963.3:p.Tyr841Phe
ENST00000328111.6:c.2546A>T MANE Select	ENSP00000328547.2:p.Tyr849Phe
ENST00000348286.6:c.2297A>T	ENSP00000337764.2:p.Tyr766Phe
ENST00000353855.6:c.2486A>T	ENSP00000313397.4:p.Tyr829Phe
ENST00000443239.7:c.2171A>T	ENSP00000403169.2:p.Tyr724Phe
ENST00000456297.6:c.2069A>T	ENSP00000412305.1:p.Tyr690Phe
NM_001207055.1:c.2171A>T	NP_001193984.1:p.Tyr724Phe
NM_001207056.1:c.2069A>T	NP_001193985.1:p.Tyr690Phe
NM_006892.3:c.2546A>T , LRG_56t1:c.2546A>T	NP_008823.1:p.Tyr849Phe
NM_175848.1:c.2486A>T	NP_787044.1:p.Tyr829Phe
NM_175849.1:c.2297A>T	NP_787045.1:p.Tyr766Phe
NM_175850.2:c.2522A>T	NP_787046.1:p.Tyr841Phe
XM_011528653.1:c.2333A>T	XP_011526955.1:p.Tyr778Phe
XM_011528654.1:c.2207A>T	XP_011526956.1:p.Tyr736Phe
XR_936511.1:n.2324A>T
XM_011528653.2:c.2333A>T	XP_011526955.1:p.Tyr778Phe
XM_011528654.2:c.2207A>T	XP_011526956.1:p.Tyr736Phe
XR_936511.2:n.2335A>T
NM_001207055.2:c.2171A>T	NP_001193984.1:p.Tyr724Phe
NM_001207056.2:c.2069A>T	NP_001193985.1:p.Tyr690Phe
NM_006892.4:c.2546A>T MANE Select	NP_008823.1:p.Tyr849Phe
NM_175848.2:c.2486A>T	NP_787044.1:p.Tyr829Phe
NM_175849.2:c.2297A>T	NP_787045.1:p.Tyr766Phe
NM_175850.3:c.2522A>T	NP_787046.1:p.Tyr841Phe