Canonical Allele Identifier: CA313159940

Gene: DNMT3B

Linked Data

• dbSNP Id: rs896816709
• gnomAD v2: 20-31395980-A-G
• gnomAD v3: 20-32808174-A-G
• gnomAD v4: 20-32808174-A-G
• MyVariant Identifiers: chr20:g.31395980A>G (hg19) ; chr20:g.32808174A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32808174A>G , CM000682.2:g.32808174A>G	GRCh38
NC_000020.10:g.31395980A>G , CM000682.1:g.31395980A>G	GRCh37
NC_000020.9:g.30859641A>G	NCBI36
NG_007290.1:g.50790A>G , LRG_56:g.50790A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1784A>G	ENSP00000512497.1:n.*1784A>G
ENST00000696232.1:c.*271A>G	ENSP00000512498.1:n.*271A>G
ENST00000696233.1:c.*1387A>G	ENSP00000512499.1:n.*1387A>G
ENST00000696238.1:c.*1576A>G	ENSP00000512502.1:n.*1576A>G
ENST00000696245.1:n.858A>G
ENST00000201963.3:c.*271A>G	ENSP00000201963.3:n.*271A>G
ENST00000328111.6:c.*271A>G MANE Select	ENSP00000328547.2:n.*271A>G
ENST00000348286.6:c.*271A>G	ENSP00000337764.2:n.*271A>G
ENST00000353855.6:c.*271A>G	ENSP00000313397.4:n.*271A>G
ENST00000443239.7:c.*271A>G	ENSP00000403169.2:n.*271A>G
NM_001207055.1:c.*271A>G	NP_001193984.1:n.*271A>G
NM_001207056.1:c.*271A>G	NP_001193985.1:n.*271A>G
NM_006892.3:c.*271A>G , LRG_56t1:c.*271A>G	NP_008823.1:n.*271A>G
NM_175848.1:c.*271A>G	NP_787044.1:n.*271A>G
NM_175849.1:c.*271A>G	NP_787045.1:n.*271A>G
NM_175850.2:c.*271A>G	NP_787046.1:n.*271A>G
XM_011528653.1:c.*271A>G	XP_011526955.1:n.*271A>G
XM_011528654.1:c.*271A>G	XP_011526956.1:n.*271A>G
XR_936511.1:n.2611A>G
XM_011528653.2:c.*271A>G	XP_011526955.1:n.*271A>G
XM_011528654.2:c.*271A>G	XP_011526956.1:n.*271A>G
XR_936511.2:n.2622A>G
NM_001207055.2:c.*271A>G	NP_001193984.1:n.*271A>G
NM_001207056.2:c.*271A>G	NP_001193985.1:n.*271A>G
NM_006892.4:c.*271A>G MANE Select	NP_008823.1:n.*271A>G
NM_175848.2:c.*271A>G	NP_787044.1:n.*271A>G
NM_175849.2:c.*271A>G	NP_787045.1:n.*271A>G
NM_175850.3:c.*271A>G	NP_787046.1:n.*271A>G