Canonical Allele Identifier: CA2360465191

Gene: DNMT3B

Linked Data

• dbSNP Id: rs1981868270
• gnomAD v4: 20-32805483-TTTGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32805487_32805490del , CM000682.2:g.32805487_32805490del	GRCh38
NC_000020.10:g.31393293_31393296del , CM000682.1:g.31393293_31393296del	GRCh37
NC_000020.9:g.30856954_30856957del	NCBI36
NG_007290.1:g.48103_48106del , LRG_56:g.48103_48106del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1252+80_*1252+83del	ENSP00000512497.1:n.*1252+80_*1252+83del
ENST00000696232.1:c.2232-2275_2232-2272del	ENSP00000512498.1:n.2232-2275_2232-2272del
ENST00000696233.1:c.*975-2275_*975-2272del	ENSP00000512499.1:n.*975-2275_*975-2272del
ENST00000696238.1:c.*1044+80_*1044+83del	ENSP00000512502.1:n.*1044+80_*1044+83del
ENST00000696239.1:c.2082+80_2082+83del	ENSP00000512503.1:n.2082+80_2082+83del
ENST00000696245.1:n.327-722_327-719del
ENST00000201963.3:c.2277+80_2277+83del	ENSP00000201963.3:n.2277+80_2277+83del
ENST00000328111.6:c.2301+80_2301+83del MANE Select	ENSP00000328547.2:n.2301+80_2301+83del
ENST00000348286.6:c.2172-2275_2172-2272del	ENSP00000337764.2:n.2172-2275_2172-2272del
ENST00000353855.6:c.2241+80_2241+83del	ENSP00000313397.4:n.2241+80_2241+83del
ENST00000443239.7:c.2046-2275_2046-2272del	ENSP00000403169.2:n.2046-2275_2046-2272del
ENST00000456297.6:c.1944-2275_1944-2272del	ENSP00000412305.1:n.1944-2275_1944-2272del
NM_001207055.1:c.2046-2275_2046-2272del	NP_001193984.1:n.2046-2275_2046-2272del
NM_001207056.1:c.1944-2275_1944-2272del	NP_001193985.1:n.1944-2275_1944-2272del
NM_006892.3:c.2301+80_2301+83del , LRG_56t1:c.2301+80_2301+83del	NP_008823.1:n.2301+80_2301+83del
NM_175848.1:c.2241+80_2241+83del	NP_787044.1:n.2241+80_2241+83del
NM_175849.1:c.2172-2275_2172-2272del	NP_787045.1:n.2172-2275_2172-2272del
NM_175850.2:c.2277+80_2277+83del	NP_787046.1:n.2277+80_2277+83del
XM_011528653.1:c.2208-2275_2208-2272del	XP_011526955.1:n.2208-2275_2208-2272del
XM_011528654.1:c.2082-2275_2082-2272del	XP_011526956.1:n.2082-2275_2082-2272del
XR_936510.1:n.2268+80_2268+83del
XR_936511.1:n.2199-2275_2199-2272del
XR_936512.1:n.2143+80_2143+83del
XM_011528653.2:c.2208-2275_2208-2272del	XP_011526955.1:n.2208-2275_2208-2272del
XM_011528654.2:c.2082-2275_2082-2272del	XP_011526956.1:n.2082-2275_2082-2272del
XR_936510.2:n.2279+80_2279+83del
XR_936511.2:n.2210-2275_2210-2272del
XR_936512.2:n.2155+80_2155+83del
NM_001207055.2:c.2046-2275_2046-2272del	NP_001193984.1:n.2046-2275_2046-2272del
NM_001207056.2:c.1944-2275_1944-2272del	NP_001193985.1:n.1944-2275_1944-2272del
NM_006892.4:c.2301+80_2301+83del MANE Select	NP_008823.1:n.2301+80_2301+83del
NM_175848.2:c.2241+80_2241+83del	NP_787044.1:n.2241+80_2241+83del
NM_175849.2:c.2172-2275_2172-2272del	NP_787045.1:n.2172-2275_2172-2272del
NM_175850.3:c.2277+80_2277+83del	NP_787046.1:n.2277+80_2277+83del