Canonical Allele Identifier: CA408592987

Gene: DNMT3B

Linked Data

• COSMIC: COSM4996006 ; COSM4996007
• MyVariant Identifiers: chr20:g.31395610G>T (hg19) ; chr20:g.32807804G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807804G>T , CM000682.2:g.32807804G>T	GRCh38
NC_000020.10:g.31395610G>T , CM000682.1:g.31395610G>T	GRCh37
NC_000020.9:g.30859271G>T	NCBI36
NG_007290.1:g.50420G>T , LRG_56:g.50420G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1414G>T	ENSP00000512497.1:n.*1414G>T
ENST00000696232.1:c.2274G>T	ENSP00000512498.1:p.Met758Ile
ENST00000696233.1:c.*1017G>T	ENSP00000512499.1:n.*1017G>T
ENST00000696238.1:c.*1206G>T	ENSP00000512502.1:n.*1206G>T
ENST00000696239.1:c.2244G>T	ENSP00000512503.1:p.Met748Ile
ENST00000696245.1:n.488G>T
ENST00000201963.3:c.2439G>T	ENSP00000201963.3:p.Met813Ile
ENST00000328111.6:c.2463G>T MANE Select	ENSP00000328547.2:p.Met821Ile
ENST00000348286.6:c.2214G>T	ENSP00000337764.2:p.Met738Ile
ENST00000353855.6:c.2403G>T	ENSP00000313397.4:p.Met801Ile
ENST00000443239.7:c.2088G>T	ENSP00000403169.2:p.Met696Ile
ENST00000456297.6:c.1986G>T	ENSP00000412305.1:p.Met662Ile
NM_001207055.1:c.2088G>T	NP_001193984.1:p.Met696Ile
NM_001207056.1:c.1986G>T	NP_001193985.1:p.Met662Ile
NM_006892.3:c.2463G>T , LRG_56t1:c.2463G>T	NP_008823.1:p.Met821Ile
NM_175848.1:c.2403G>T	NP_787044.1:p.Met801Ile
NM_175849.1:c.2214G>T	NP_787045.1:p.Met738Ile
NM_175850.2:c.2439G>T	NP_787046.1:p.Met813Ile
XM_011528653.1:c.2250G>T	XP_011526955.1:p.Met750Ile
XM_011528654.1:c.2124G>T	XP_011526956.1:p.Met708Ile
XR_936511.1:n.2241G>T
XM_011528653.2:c.2250G>T	XP_011526955.1:p.Met750Ile
XM_011528654.2:c.2124G>T	XP_011526956.1:p.Met708Ile
XR_936511.2:n.2252G>T
NM_001207055.2:c.2088G>T	NP_001193984.1:p.Met696Ile
NM_001207056.2:c.1986G>T	NP_001193985.1:p.Met662Ile
NM_006892.4:c.2463G>T MANE Select	NP_008823.1:p.Met821Ile
NM_175848.2:c.2403G>T	NP_787044.1:p.Met801Ile
NM_175849.2:c.2214G>T	NP_787045.1:p.Met738Ile
NM_175850.3:c.2439G>T	NP_787046.1:p.Met813Ile