Canonical Allele Identifier: CA10652469

Gene: DNMT3B

Linked Data

• ClinVar Variation Id: 338194
• ClinVar RCV Id: RCV000353066
• dbSNP Id: rs886056623
• MyVariant Identifiers: chr20:g.31396286C>T (hg19) ; chr20:g.32808480C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32808480C>T , CM000682.2:g.32808480C>T	GRCh38
NC_000020.10:g.31396286C>T , CM000682.1:g.31396286C>T	GRCh37
NC_000020.9:g.30859947C>T	NCBI36
NG_007290.1:g.51096C>T , LRG_56:g.51096C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*2090C>T	ENSP00000512497.1:n.*2090C>T
ENST00000696232.1:c.*577C>T	ENSP00000512498.1:n.*577C>T
ENST00000696233.1:c.*1693C>T	ENSP00000512499.1:n.*1693C>T
ENST00000696238.1:c.*1882C>T	ENSP00000512502.1:n.*1882C>T
ENST00000696245.1:n.1164C>T
ENST00000201963.3:c.*577C>T	ENSP00000201963.3:n.*577C>T
ENST00000328111.6:c.*577C>T MANE Select	ENSP00000328547.2:n.*577C>T
ENST00000348286.6:c.*577C>T	ENSP00000337764.2:n.*577C>T
ENST00000353855.6:c.*577C>T	ENSP00000313397.4:n.*577C>T
NM_001207055.1:c.*577C>T	NP_001193984.1:n.*577C>T
NM_001207056.1:c.*577C>T	NP_001193985.1:n.*577C>T
NM_006892.3:c.*577C>T , LRG_56t1:c.*577C>T	NP_008823.1:n.*577C>T
NM_175848.1:c.*577C>T	NP_787044.1:n.*577C>T
NM_175849.1:c.*577C>T	NP_787045.1:n.*577C>T
NM_175850.2:c.*577C>T	NP_787046.1:n.*577C>T
XM_011528653.1:c.*577C>T	XP_011526955.1:n.*577C>T
XM_011528654.1:c.*577C>T	XP_011526956.1:n.*577C>T
XR_936511.1:n.2917C>T
XM_011528653.2:c.*577C>T	XP_011526955.1:n.*577C>T
XM_011528654.2:c.*577C>T	XP_011526956.1:n.*577C>T
XR_936511.2:n.2928C>T
NM_001207055.2:c.*577C>T	NP_001193984.1:n.*577C>T
NM_001207056.2:c.*577C>T	NP_001193985.1:n.*577C>T
NM_006892.4:c.*577C>T MANE Select	NP_008823.1:n.*577C>T
NM_175848.2:c.*577C>T	NP_787044.1:n.*577C>T
NM_175849.2:c.*577C>T	NP_787045.1:n.*577C>T
NM_175850.3:c.*577C>T	NP_787046.1:n.*577C>T