Canonical Allele Identifier: CA408592973

Gene: DNMT3B

Linked Data

• dbSNP Id: rs1982134161
• MyVariant Identifiers: chr20:g.31395608A>C (hg19) ; chr20:g.32807802A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807802A>C , CM000682.2:g.32807802A>C	GRCh38
NC_000020.10:g.31395608A>C , CM000682.1:g.31395608A>C	GRCh37
NC_000020.9:g.30859269A>C	NCBI36
NG_007290.1:g.50418A>C , LRG_56:g.50418A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1412A>C	ENSP00000512497.1:n.*1412A>C
ENST00000696232.1:c.2272A>C	ENSP00000512498.1:p.Met758Leu
ENST00000696233.1:c.*1015A>C	ENSP00000512499.1:n.*1015A>C
ENST00000696238.1:c.*1204A>C	ENSP00000512502.1:n.*1204A>C
ENST00000696239.1:c.2242A>C	ENSP00000512503.1:p.Met748Leu
ENST00000696245.1:n.486A>C
ENST00000201963.3:c.2437A>C	ENSP00000201963.3:p.Met813Leu
ENST00000328111.6:c.2461A>C MANE Select	ENSP00000328547.2:p.Met821Leu
ENST00000348286.6:c.2212A>C	ENSP00000337764.2:p.Met738Leu
ENST00000353855.6:c.2401A>C	ENSP00000313397.4:p.Met801Leu
ENST00000443239.7:c.2086A>C	ENSP00000403169.2:p.Met696Leu
ENST00000456297.6:c.1984A>C	ENSP00000412305.1:p.Met662Leu
NM_001207055.1:c.2086A>C	NP_001193984.1:p.Met696Leu
NM_001207056.1:c.1984A>C	NP_001193985.1:p.Met662Leu
NM_006892.3:c.2461A>C , LRG_56t1:c.2461A>C	NP_008823.1:p.Met821Leu
NM_175848.1:c.2401A>C	NP_787044.1:p.Met801Leu
NM_175849.1:c.2212A>C	NP_787045.1:p.Met738Leu
NM_175850.2:c.2437A>C	NP_787046.1:p.Met813Leu
XM_011528653.1:c.2248A>C	XP_011526955.1:p.Met750Leu
XM_011528654.1:c.2122A>C	XP_011526956.1:p.Met708Leu
XR_936511.1:n.2239A>C
XM_011528653.2:c.2248A>C	XP_011526955.1:p.Met750Leu
XM_011528654.2:c.2122A>C	XP_011526956.1:p.Met708Leu
XR_936511.2:n.2250A>C
NM_001207055.2:c.2086A>C	NP_001193984.1:p.Met696Leu
NM_001207056.2:c.1984A>C	NP_001193985.1:p.Met662Leu
NM_006892.4:c.2461A>C MANE Select	NP_008823.1:p.Met821Leu
NM_175848.2:c.2401A>C	NP_787044.1:p.Met801Leu
NM_175849.2:c.2212A>C	NP_787045.1:p.Met738Leu
NM_175850.3:c.2437A>C	NP_787046.1:p.Met813Leu