Canonical Allele Identifier: CA313159952

Gene: DNMT3B

Linked Data

• dbSNP Id: rs1024509449
• gnomAD v4: 20-32808193-T-C
• MyVariant Identifiers: chr20:g.31395999T>C (hg19) ; chr20:g.32808193T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32808193T>C , CM000682.2:g.32808193T>C	GRCh38
NC_000020.10:g.31395999T>C , CM000682.1:g.31395999T>C	GRCh37
NC_000020.9:g.30859660T>C	NCBI36
NG_007290.1:g.50809T>C , LRG_56:g.50809T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1803T>C	ENSP00000512497.1:n.*1803T>C
ENST00000696232.1:c.*290T>C	ENSP00000512498.1:n.*290T>C
ENST00000696233.1:c.*1406T>C	ENSP00000512499.1:n.*1406T>C
ENST00000696238.1:c.*1595T>C	ENSP00000512502.1:n.*1595T>C
ENST00000696245.1:n.877T>C
ENST00000201963.3:c.*290T>C	ENSP00000201963.3:n.*290T>C
ENST00000328111.6:c.*290T>C MANE Select	ENSP00000328547.2:n.*290T>C
ENST00000348286.6:c.*290T>C	ENSP00000337764.2:n.*290T>C
ENST00000353855.6:c.*290T>C	ENSP00000313397.4:n.*290T>C
ENST00000443239.7:c.*290T>C	ENSP00000403169.2:n.*290T>C
NM_001207055.1:c.*290T>C	NP_001193984.1:n.*290T>C
NM_001207056.1:c.*290T>C	NP_001193985.1:n.*290T>C
NM_006892.3:c.*290T>C , LRG_56t1:c.*290T>C	NP_008823.1:n.*290T>C
NM_175848.1:c.*290T>C	NP_787044.1:n.*290T>C
NM_175849.1:c.*290T>C	NP_787045.1:n.*290T>C
NM_175850.2:c.*290T>C	NP_787046.1:n.*290T>C
XM_011528653.1:c.*290T>C	XP_011526955.1:n.*290T>C
XM_011528654.1:c.*290T>C	XP_011526956.1:n.*290T>C
XR_936511.1:n.2630T>C
XM_011528653.2:c.*290T>C	XP_011526955.1:n.*290T>C
XM_011528654.2:c.*290T>C	XP_011526956.1:n.*290T>C
XR_936511.2:n.2641T>C
NM_001207055.2:c.*290T>C	NP_001193984.1:n.*290T>C
NM_001207056.2:c.*290T>C	NP_001193985.1:n.*290T>C
NM_006892.4:c.*290T>C MANE Select	NP_008823.1:n.*290T>C
NM_175848.2:c.*290T>C	NP_787044.1:n.*290T>C
NM_175849.2:c.*290T>C	NP_787045.1:n.*290T>C
NM_175850.3:c.*290T>C	NP_787046.1:n.*290T>C