Canonical Allele Identifier: CA743667171

Gene: DNMT3B

Linked Data

• dbSNP Id: rs1187989912
• gnomAD v3: 20-32805456-G-C
• gnomAD v4: 20-32805456-G-C
• MyVariant Identifiers: chr20:g.31393262G>C (hg19) ; chr20:g.32805456G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32805456G>C , CM000682.2:g.32805456G>C	GRCh38
NC_000020.10:g.31393262G>C , CM000682.1:g.31393262G>C	GRCh37
NC_000020.9:g.30856923G>C	NCBI36
NG_007290.1:g.48072G>C , LRG_56:g.48072G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1252+49G>C	ENSP00000512497.1:n.*1252+49G>C
ENST00000696232.1:c.2232-2306G>C	ENSP00000512498.1:n.2232-2306G>C
ENST00000696233.1:c.*975-2306G>C	ENSP00000512499.1:n.*975-2306G>C
ENST00000696238.1:c.*1044+49G>C	ENSP00000512502.1:n.*1044+49G>C
ENST00000696239.1:c.2082+49G>C	ENSP00000512503.1:n.2082+49G>C
ENST00000696245.1:n.327-753G>C
ENST00000201963.3:c.2277+49G>C	ENSP00000201963.3:n.2277+49G>C
ENST00000328111.6:c.2301+49G>C MANE Select	ENSP00000328547.2:n.2301+49G>C
ENST00000348286.6:c.2172-2306G>C	ENSP00000337764.2:n.2172-2306G>C
ENST00000353855.6:c.2241+49G>C	ENSP00000313397.4:n.2241+49G>C
ENST00000443239.7:c.2046-2306G>C	ENSP00000403169.2:n.2046-2306G>C
ENST00000456297.6:c.1944-2306G>C	ENSP00000412305.1:n.1944-2306G>C
NM_001207055.1:c.2046-2306G>C	NP_001193984.1:n.2046-2306G>C
NM_001207056.1:c.1944-2306G>C	NP_001193985.1:n.1944-2306G>C
NM_006892.3:c.2301+49G>C , LRG_56t1:c.2301+49G>C	NP_008823.1:n.2301+49G>C
NM_175848.1:c.2241+49G>C	NP_787044.1:n.2241+49G>C
NM_175849.1:c.2172-2306G>C	NP_787045.1:n.2172-2306G>C
NM_175850.2:c.2277+49G>C	NP_787046.1:n.2277+49G>C
XM_011528653.1:c.2208-2306G>C	XP_011526955.1:n.2208-2306G>C
XM_011528654.1:c.2082-2306G>C	XP_011526956.1:n.2082-2306G>C
XR_936510.1:n.2268+49G>C
XR_936511.1:n.2199-2306G>C
XR_936512.1:n.2143+49G>C
XM_011528653.2:c.2208-2306G>C	XP_011526955.1:n.2208-2306G>C
XM_011528654.2:c.2082-2306G>C	XP_011526956.1:n.2082-2306G>C
XR_936510.2:n.2279+49G>C
XR_936511.2:n.2210-2306G>C
XR_936512.2:n.2155+49G>C
NM_001207055.2:c.2046-2306G>C	NP_001193984.1:n.2046-2306G>C
NM_001207056.2:c.1944-2306G>C	NP_001193985.1:n.1944-2306G>C
NM_006892.4:c.2301+49G>C MANE Select	NP_008823.1:n.2301+49G>C
NM_175848.2:c.2241+49G>C	NP_787044.1:n.2241+49G>C
NM_175849.2:c.2172-2306G>C	NP_787045.1:n.2172-2306G>C
NM_175850.3:c.2277+49G>C	NP_787046.1:n.2277+49G>C