Canonical Allele Identifier: CA408586534
Gene: DNMT3B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32787290T>G , CM000682.2:g.32787290T>G GRCh38
NC_000020.10:g.31375096T>G , CM000682.1:g.31375096T>G GRCh37
NC_000020.9:g.30838757T>G NCBI36
NG_007290.1:g.29906T>G , LRG_56:g.29906T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.493T>G ENSP00000512497.1:p.Tyr165Asp
ENST00000696232.1:c.493T>G ENSP00000512498.1:p.Tyr165Asp
ENST00000696233.1:c.493T>G ENSP00000512499.1:p.Tyr165Asp
ENST00000696234.1:n.477T>G
ENST00000696235.1:c.367T>G ENSP00000512500.1:p.Tyr123Asp
ENST00000696236.1:c.367T>G ENSP00000512501.1:p.Tyr123Asp
ENST00000696237.1:n.599T>G
ENST00000696238.1:c.493T>G ENSP00000512502.1:p.Tyr165Asp
ENST00000696239.1:c.493T>G ENSP00000512503.1:p.Tyr165Asp
ENST00000201963.3:c.529T>G ENSP00000201963.3:p.Tyr177Asp
ENST00000328111.6:c.493T>G MANE Select ENSP00000328547.2:p.Tyr165Asp
ENST00000348286.6:c.493T>G ENSP00000337764.2:p.Tyr165Asp
ENST00000353855.6:c.493T>G ENSP00000313397.4:p.Tyr165Asp
ENST00000443239.7:c.367T>G ENSP00000403169.2:p.Tyr123Asp
ENST00000456297.6:c.265T>G ENSP00000412305.1:p.Tyr89Asp
NM_001207055.1:c.367T>G NP_001193984.1:p.Tyr123Asp
NM_001207056.1:c.265T>G NP_001193985.1:p.Tyr89Asp
NM_006892.3:c.493T>G , LRG_56t1:c.493T>G NP_008823.1:p.Tyr165Asp
NM_175848.1:c.493T>G NP_787044.1:p.Tyr165Asp
NM_175849.1:c.493T>G NP_787045.1:p.Tyr165Asp
NM_175850.2:c.529T>G NP_787046.1:p.Tyr177Asp
XM_011528653.1:c.529T>G XP_011526955.1:p.Tyr177Asp
XM_011528654.1:c.403T>G XP_011526956.1:p.Tyr135Asp
XR_936510.1:n.665T>G
XR_936511.1:n.665T>G
XR_936512.1:n.540T>G
XM_011528653.2:c.529T>G XP_011526955.1:p.Tyr177Asp
XM_011528654.2:c.403T>G XP_011526956.1:p.Tyr135Asp
XR_936510.2:n.676T>G
XR_936511.2:n.676T>G
XR_936512.2:n.552T>G
NM_001207055.2:c.367T>G NP_001193984.1:p.Tyr123Asp
NM_001207056.2:c.265T>G NP_001193985.1:p.Tyr89Asp
NM_006892.4:c.493T>G MANE Select NP_008823.1:p.Tyr165Asp
NM_175848.2:c.493T>G NP_787044.1:p.Tyr165Asp
NM_175849.2:c.493T>G NP_787045.1:p.Tyr165Asp
NM_175850.3:c.529T>G NP_787046.1:p.Tyr177Asp