Canonical Allele Identifier: CA408593035

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31395623C>G (hg19) ; chr20:g.32807817C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807817C>G , CM000682.2:g.32807817C>G	GRCh38
NC_000020.10:g.31395623C>G , CM000682.1:g.31395623C>G	GRCh37
NC_000020.9:g.30859284C>G	NCBI36
NG_007290.1:g.50433C>G , LRG_56:g.50433C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1427C>G	ENSP00000512497.1:n.*1427C>G
ENST00000696232.1:c.2287C>G	ENSP00000512498.1:p.Arg763Gly
ENST00000696233.1:c.*1030C>G	ENSP00000512499.1:n.*1030C>G
ENST00000696238.1:c.*1219C>G	ENSP00000512502.1:n.*1219C>G
ENST00000696239.1:c.2257C>G	ENSP00000512503.1:p.Arg753Gly
ENST00000696245.1:n.501C>G
ENST00000201963.3:c.2452C>G	ENSP00000201963.3:p.Arg818Gly
ENST00000328111.6:c.2476C>G MANE Select	ENSP00000328547.2:p.Arg826Gly
ENST00000348286.6:c.2227C>G	ENSP00000337764.2:p.Arg743Gly
ENST00000353855.6:c.2416C>G	ENSP00000313397.4:p.Arg806Gly
ENST00000443239.7:c.2101C>G	ENSP00000403169.2:p.Arg701Gly
ENST00000456297.6:c.1999C>G	ENSP00000412305.1:p.Arg667Gly
NM_001207055.1:c.2101C>G	NP_001193984.1:p.Arg701Gly
NM_001207056.1:c.1999C>G	NP_001193985.1:p.Arg667Gly
NM_006892.3:c.2476C>G , LRG_56t1:c.2476C>G	NP_008823.1:p.Arg826Gly
NM_175848.1:c.2416C>G	NP_787044.1:p.Arg806Gly
NM_175849.1:c.2227C>G	NP_787045.1:p.Arg743Gly
NM_175850.2:c.2452C>G	NP_787046.1:p.Arg818Gly
XM_011528653.1:c.2263C>G	XP_011526955.1:p.Arg755Gly
XM_011528654.1:c.2137C>G	XP_011526956.1:p.Arg713Gly
XR_936511.1:n.2254C>G
XM_011528653.2:c.2263C>G	XP_011526955.1:p.Arg755Gly
XM_011528654.2:c.2137C>G	XP_011526956.1:p.Arg713Gly
XR_936511.2:n.2265C>G
NM_001207055.2:c.2101C>G	NP_001193984.1:p.Arg701Gly
NM_001207056.2:c.1999C>G	NP_001193985.1:p.Arg667Gly
NM_006892.4:c.2476C>G MANE Select	NP_008823.1:p.Arg826Gly
NM_175848.2:c.2416C>G	NP_787044.1:p.Arg806Gly
NM_175849.2:c.2227C>G	NP_787045.1:p.Arg743Gly
NM_175850.3:c.2452C>G	NP_787046.1:p.Arg818Gly