Canonical Allele Identifier: CA408592097

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31393154G>T (hg19) ; chr20:g.32805348G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32805348G>T , CM000682.2:g.32805348G>T	GRCh38
NC_000020.10:g.31393154G>T , CM000682.1:g.31393154G>T	GRCh37
NC_000020.9:g.30856815G>T	NCBI36
NG_007290.1:g.47964G>T , LRG_56:g.47964G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696231.1:c.*1193G>T	ENSP00000512497.1:n.*1193G>T
ENST00000696232.1:c.2232-2414G>T	ENSP00000512498.1:n.2232-2414G>T
ENST00000696233.1:c.*975-2414G>T	ENSP00000512499.1:n.*975-2414G>T
ENST00000696238.1:c.*985G>T	ENSP00000512502.1:n.*985G>T
ENST00000696239.1:c.2023G>T	ENSP00000512503.1:p.Ala675Ser
ENST00000696245.1:n.327-861G>T
ENST00000201963.3:c.2218G>T	ENSP00000201963.3:p.Ala740Ser
ENST00000328111.6:c.2242G>T MANE Select	ENSP00000328547.2:p.Ala748Ser
ENST00000348286.6:c.2172-2414G>T	ENSP00000337764.2:n.2172-2414G>T
ENST00000353855.6:c.2182G>T	ENSP00000313397.4:p.Ala728Ser
ENST00000443239.7:c.2046-2414G>T	ENSP00000403169.2:n.2046-2414G>T
ENST00000456297.6:c.1944-2414G>T	ENSP00000412305.1:n.1944-2414G>T
NM_001207055.1:c.2046-2414G>T	NP_001193984.1:n.2046-2414G>T
NM_001207056.1:c.1944-2414G>T	NP_001193985.1:n.1944-2414G>T
NM_006892.3:c.2242G>T , LRG_56t1:c.2242G>T	NP_008823.1:p.Ala748Ser
NM_175848.1:c.2182G>T	NP_787044.1:p.Ala728Ser
NM_175849.1:c.2172-2414G>T	NP_787045.1:n.2172-2414G>T
NM_175850.2:c.2218G>T	NP_787046.1:p.Ala740Ser
XM_011528653.1:c.2208-2414G>T	XP_011526955.1:n.2208-2414G>T
XM_011528654.1:c.2082-2414G>T	XP_011526956.1:n.2082-2414G>T
XR_936510.1:n.2209G>T
XR_936511.1:n.2199-2414G>T
XR_936512.1:n.2084G>T
XM_011528653.2:c.2208-2414G>T	XP_011526955.1:n.2208-2414G>T
XM_011528654.2:c.2082-2414G>T	XP_011526956.1:n.2082-2414G>T
XR_936510.2:n.2220G>T
XR_936511.2:n.2210-2414G>T
XR_936512.2:n.2096G>T
NM_001207055.2:c.2046-2414G>T	NP_001193984.1:n.2046-2414G>T
NM_001207056.2:c.1944-2414G>T	NP_001193985.1:n.1944-2414G>T
NM_006892.4:c.2242G>T MANE Select	NP_008823.1:p.Ala748Ser
NM_175848.2:c.2182G>T	NP_787044.1:p.Ala728Ser
NM_175849.2:c.2172-2414G>T	NP_787045.1:n.2172-2414G>T
NM_175850.3:c.2218G>T	NP_787046.1:p.Ala740Ser