Canonical Allele Identifier: CA510214564

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31395673C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807867C>G , CM000682.2:g.32807867C>G	GRCh38
NC_000020.10:g.31395673C>G , CM000682.1:g.31395673C>G	GRCh37
NC_000020.9:g.30859334C>G	NCBI36
NG_007290.1:g.50483C>G , LRG_56:g.50483C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696231.1:c.*1477C>G	ENSP00000512497.1:n.*1477C>G
ENST00000696232.1:c.2337C>G	ENSP00000512498.1:p.Leu779=
ENST00000696233.1:c.*1080C>G	ENSP00000512499.1:n.*1080C>G
ENST00000696238.1:c.*1269C>G	ENSP00000512502.1:n.*1269C>G
ENST00000696239.1:c.2307C>G	ENSP00000512503.1:p.Leu769=
ENST00000696245.1:n.551C>G
ENST00000201963.3:c.2502C>G	ENSP00000201963.3:p.Leu834=
ENST00000328111.6:c.2526C>G MANE Select	ENSP00000328547.2:p.Leu842=
ENST00000348286.6:c.2277C>G	ENSP00000337764.2:p.Leu759=
ENST00000353855.6:c.2466C>G	ENSP00000313397.4:p.Leu822=
ENST00000443239.7:c.2151C>G	ENSP00000403169.2:p.Leu717=
ENST00000456297.6:c.2049C>G	ENSP00000412305.1:p.Leu683=
NM_001207055.1:c.2151C>G	NP_001193984.1:p.Leu717=
NM_001207056.1:c.2049C>G	NP_001193985.1:p.Leu683=
NM_006892.3:c.2526C>G , LRG_56t1:c.2526C>G	NP_008823.1:p.Leu842=
NM_175848.1:c.2466C>G	NP_787044.1:p.Leu822=
NM_175849.1:c.2277C>G	NP_787045.1:p.Leu759=
NM_175850.2:c.2502C>G	NP_787046.1:p.Leu834=
XM_011528653.1:c.2313C>G	XP_011526955.1:p.Leu771=
XM_011528654.1:c.2187C>G	XP_011526956.1:p.Leu729=
XR_936511.1:n.2304C>G
XM_011528653.2:c.2313C>G	XP_011526955.1:p.Leu771=
XM_011528654.2:c.2187C>G	XP_011526956.1:p.Leu729=
XR_936511.2:n.2315C>G
NM_001207055.2:c.2151C>G	NP_001193984.1:p.Leu717=
NM_001207056.2:c.2049C>G	NP_001193985.1:p.Leu683=
NM_006892.4:c.2526C>G MANE Select	NP_008823.1:p.Leu842=
NM_175848.2:c.2466C>G	NP_787044.1:p.Leu822=
NM_175849.2:c.2277C>G	NP_787045.1:p.Leu759=
NM_175850.3:c.2502C>G	NP_787046.1:p.Leu834=