Canonical Allele Identifier: CA9810137

Gene: DNMT3B

Linked Data

• ClinVar Variation Id: 1170168
• ClinVar RCV Id: RCV001522267
• dbSNP Id: rs2424913
• ExAC: 20:31374259 C / T
• gnomAD v2: 20-31374259-C-T
• gnomAD v3: 20-32786453-C-T
• gnomAD v4: 20-32786453-C-T
• MyVariant Identifiers: chr20:g.31374259C>T (hg19) ; chr20:g.32786453C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32786453C>T , CM000682.2:g.32786453C>T	GRCh38
NC_000020.10:g.31374259C>T , CM000682.1:g.31374259C>T	GRCh37
NC_000020.9:g.30837920C>T	NCBI36
NG_007290.1:g.29069C>T , LRG_56:g.29069C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696231.1:c.307-49C>T	ENSP00000512497.1:n.307-49C>T
ENST00000696232.1:c.307-49C>T	ENSP00000512498.1:n.307-49C>T
ENST00000696233.1:c.307-49C>T	ENSP00000512499.1:n.307-49C>T
ENST00000696234.1:n.417-777C>T
ENST00000696235.1:c.307-777C>T	ENSP00000512500.1:n.307-777C>T
ENST00000696236.1:c.307-777C>T	ENSP00000512501.1:n.307-777C>T
ENST00000696237.1:n.413-49C>T
ENST00000696238.1:c.307-49C>T	ENSP00000512502.1:n.307-49C>T
ENST00000696239.1:c.307-49C>T	ENSP00000512503.1:n.307-49C>T
ENST00000201963.3:c.343-49C>T	ENSP00000201963.3:n.343-49C>T
ENST00000328111.6:c.307-49C>T MANE Select	ENSP00000328547.2:n.307-49C>T
ENST00000348286.6:c.307-49C>T	ENSP00000337764.2:n.307-49C>T
ENST00000353855.6:c.307-49C>T	ENSP00000313397.4:n.307-49C>T
ENST00000443239.7:c.307-777C>T	ENSP00000403169.2:n.307-777C>T
ENST00000456297.6:c.205-777C>T	ENSP00000412305.1:n.205-777C>T
NM_001207055.1:c.307-777C>T	NP_001193984.1:n.307-777C>T
NM_001207056.1:c.205-777C>T	NP_001193985.1:n.205-777C>T
NM_006892.3:c.307-49C>T , LRG_56t1:c.307-49C>T	NP_008823.1:n.307-49C>T
NM_175848.1:c.307-49C>T	NP_787044.1:n.307-49C>T
NM_175849.1:c.307-49C>T	NP_787045.1:n.307-49C>T
NM_175850.2:c.343-49C>T	NP_787046.1:n.343-49C>T
XM_011528653.1:c.343-49C>T	XP_011526955.1:n.343-49C>T
XM_011528654.1:c.343-777C>T	XP_011526956.1:n.343-777C>T
XR_936510.1:n.479-49C>T
XR_936511.1:n.479-49C>T
XR_936512.1:n.480-777C>T
XM_011528653.2:c.343-49C>T	XP_011526955.1:n.343-49C>T
XM_011528654.2:c.343-777C>T	XP_011526956.1:n.343-777C>T
XR_936510.2:n.490-49C>T
XR_936511.2:n.490-49C>T
XR_936512.2:n.492-777C>T
NM_001207055.2:c.307-777C>T	NP_001193984.1:n.307-777C>T
NM_001207056.2:c.205-777C>T	NP_001193985.1:n.205-777C>T
NM_006892.4:c.307-49C>T MANE Select	NP_008823.1:n.307-49C>T
NM_175848.2:c.307-49C>T	NP_787044.1:n.307-49C>T
NM_175849.2:c.307-49C>T	NP_787045.1:n.307-49C>T
NM_175850.3:c.343-49C>T	NP_787046.1:n.343-49C>T