Canonical Allele Identifier: CA10653070

Gene: DNMT3B

Linked Data

• ClinVar Variation Id: 338190
• ClinVar RCV Id: RCV000282840
• dbSNP Id: rs886056621
• MyVariant Identifiers: chr20:g.31395954dupT (hg19) ; chr20:g.32808148dupT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32808148dup , CM000682.2:g.32808148dup	GRCh38
NC_000020.10:g.31395954dup , CM000682.1:g.31395954dup	GRCh37
NC_000020.9:g.30859615dup	NCBI36
NG_007290.1:g.50764dup , LRG_56:g.50764dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1758dup	ENSP00000512497.1:n.*1758dup
ENST00000696232.1:c.*245dup	ENSP00000512498.1:n.*245dup
ENST00000696233.1:c.*1361dup	ENSP00000512499.1:n.*1361dup
ENST00000696238.1:c.*1550dup	ENSP00000512502.1:n.*1550dup
ENST00000696245.1:n.832dup
ENST00000201963.3:c.*245dup	ENSP00000201963.3:n.*245dup
ENST00000328111.6:c.*245dup MANE Select	ENSP00000328547.2:n.*245dup
ENST00000348286.6:c.*245dup	ENSP00000337764.2:n.*245dup
ENST00000353855.6:c.*245dup	ENSP00000313397.4:n.*245dup
ENST00000443239.7:c.*245dup	ENSP00000403169.2:n.*245dup
NM_001207055.1:c.*245dup	NP_001193984.1:n.*245dup
NM_001207056.1:c.*245dup	NP_001193985.1:n.*245dup
NM_006892.3:c.*245dup , LRG_56t1:c.*245dup	NP_008823.1:n.*245dup
NM_175848.1:c.*245dup	NP_787044.1:n.*245dup
NM_175849.1:c.*245dup	NP_787045.1:n.*245dup
NM_175850.2:c.*245dup	NP_787046.1:n.*245dup
XM_011528653.1:c.*245dup	XP_011526955.1:n.*245dup
XM_011528654.1:c.*245dup	XP_011526956.1:n.*245dup
XR_936511.1:n.2585dup
XM_011528653.2:c.*245dup	XP_011526955.1:n.*245dup
XM_011528654.2:c.*245dup	XP_011526956.1:n.*245dup
XR_936511.2:n.2596dup
NM_001207055.2:c.*245dup	NP_001193984.1:n.*245dup
NM_001207056.2:c.*245dup	NP_001193985.1:n.*245dup
NM_006892.4:c.*245dup MANE Select	NP_008823.1:n.*245dup
NM_175848.2:c.*245dup	NP_787044.1:n.*245dup
NM_175849.2:c.*245dup	NP_787045.1:n.*245dup
NM_175850.3:c.*245dup	NP_787046.1:n.*245dup