Canonical Allele Identifier: CA510212127
Gene: DNMT3B HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.31393207A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32805401A>T , CM000682.2:g.32805401A>T GRCh38
NC_000020.10:g.31393207A>T , CM000682.1:g.31393207A>T GRCh37
NC_000020.9:g.30856868A>T NCBI36
NG_007290.1:g.48017A>T , LRG_56:g.48017A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.*1246A>T ENSP00000512497.1:n.*1246A>T
ENST00000696232.1:c.2232-2361A>T ENSP00000512498.1:n.2232-2361A>T
ENST00000696233.1:c.*975-2361A>T ENSP00000512499.1:n.*975-2361A>T
ENST00000696238.1:c.*1038A>T ENSP00000512502.1:n.*1038A>T
ENST00000696239.1:c.2076A>T ENSP00000512503.1:p.Ile692=
ENST00000696245.1:n.327-808A>T
ENST00000201963.3:c.2271A>T ENSP00000201963.3:p.Ile757=
ENST00000328111.6:c.2295A>T MANE Select ENSP00000328547.2:p.Ile765=
ENST00000348286.6:c.2172-2361A>T ENSP00000337764.2:n.2172-2361A>T
ENST00000353855.6:c.2235A>T ENSP00000313397.4:p.Ile745=
ENST00000443239.7:c.2046-2361A>T ENSP00000403169.2:n.2046-2361A>T
ENST00000456297.6:c.1944-2361A>T ENSP00000412305.1:n.1944-2361A>T
NM_001207055.1:c.2046-2361A>T NP_001193984.1:n.2046-2361A>T
NM_001207056.1:c.1944-2361A>T NP_001193985.1:n.1944-2361A>T
NM_006892.3:c.2295A>T , LRG_56t1:c.2295A>T NP_008823.1:p.Ile765=
NM_175848.1:c.2235A>T NP_787044.1:p.Ile745=
NM_175849.1:c.2172-2361A>T NP_787045.1:n.2172-2361A>T
NM_175850.2:c.2271A>T NP_787046.1:p.Ile757=
XM_011528653.1:c.2208-2361A>T XP_011526955.1:n.2208-2361A>T
XM_011528654.1:c.2082-2361A>T XP_011526956.1:n.2082-2361A>T
XR_936510.1:n.2262A>T
XR_936511.1:n.2199-2361A>T
XR_936512.1:n.2137A>T
XM_011528653.2:c.2208-2361A>T XP_011526955.1:n.2208-2361A>T
XM_011528654.2:c.2082-2361A>T XP_011526956.1:n.2082-2361A>T
XR_936510.2:n.2273A>T
XR_936511.2:n.2210-2361A>T
XR_936512.2:n.2149A>T
NM_001207055.2:c.2046-2361A>T NP_001193984.1:n.2046-2361A>T
NM_001207056.2:c.1944-2361A>T NP_001193985.1:n.1944-2361A>T
NM_006892.4:c.2295A>T MANE Select NP_008823.1:p.Ile765=
NM_175848.2:c.2235A>T NP_787044.1:p.Ile745=
NM_175849.2:c.2172-2361A>T NP_787045.1:n.2172-2361A>T
NM_175850.3:c.2271A>T NP_787046.1:p.Ile757=