Canonical Allele Identifier: CA510214611

Gene: DNMT3B

Linked Data

• dbSNP Id: rs1189646152
• gnomAD v3: 20-32807879-G-A
• gnomAD v4: 20-32807879-G-A
• MyVariant Identifiers: chr20:g.31395685G>A (hg19) ; chr20:g.32807879G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807879G>A , CM000682.2:g.32807879G>A	GRCh38
NC_000020.10:g.31395685G>A , CM000682.1:g.31395685G>A	GRCh37
NC_000020.9:g.30859346G>A	NCBI36
NG_007290.1:g.50495G>A , LRG_56:g.50495G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1489G>A	ENSP00000512497.1:n.*1489G>A
ENST00000696232.1:c.2349G>A	ENSP00000512498.1:p.Leu783=
ENST00000696233.1:c.*1092G>A	ENSP00000512499.1:n.*1092G>A
ENST00000696238.1:c.*1281G>A	ENSP00000512502.1:n.*1281G>A
ENST00000696239.1:c.2319G>A	ENSP00000512503.1:p.Leu773=
ENST00000696245.1:n.563G>A
ENST00000201963.3:c.2514G>A	ENSP00000201963.3:p.Leu838=
ENST00000328111.6:c.2538G>A MANE Select	ENSP00000328547.2:p.Leu846=
ENST00000348286.6:c.2289G>A	ENSP00000337764.2:p.Leu763=
ENST00000353855.6:c.2478G>A	ENSP00000313397.4:p.Leu826=
ENST00000443239.7:c.2163G>A	ENSP00000403169.2:p.Leu721=
ENST00000456297.6:c.2061G>A	ENSP00000412305.1:p.Leu687=
NM_001207055.1:c.2163G>A	NP_001193984.1:p.Leu721=
NM_001207056.1:c.2061G>A	NP_001193985.1:p.Leu687=
NM_006892.3:c.2538G>A , LRG_56t1:c.2538G>A	NP_008823.1:p.Leu846=
NM_175848.1:c.2478G>A	NP_787044.1:p.Leu826=
NM_175849.1:c.2289G>A	NP_787045.1:p.Leu763=
NM_175850.2:c.2514G>A	NP_787046.1:p.Leu838=
XM_011528653.1:c.2325G>A	XP_011526955.1:p.Leu775=
XM_011528654.1:c.2199G>A	XP_011526956.1:p.Leu733=
XR_936511.1:n.2316G>A
XM_011528653.2:c.2325G>A	XP_011526955.1:p.Leu775=
XM_011528654.2:c.2199G>A	XP_011526956.1:p.Leu733=
XR_936511.2:n.2327G>A
NM_001207055.2:c.2163G>A	NP_001193984.1:p.Leu721=
NM_001207056.2:c.2061G>A	NP_001193985.1:p.Leu687=
NM_006892.4:c.2538G>A MANE Select	NP_008823.1:p.Leu846=
NM_175848.2:c.2478G>A	NP_787044.1:p.Leu826=
NM_175849.2:c.2289G>A	NP_787045.1:p.Leu763=
NM_175850.3:c.2514G>A	NP_787046.1:p.Leu838=