Canonical Allele Identifier: CA408588532

Gene: DNMT3B

Linked Data

• gnomAD v4: 20-32800281-A-G
• MyVariant Identifiers: chr20:g.31388087A>G (hg19) ; chr20:g.32800281A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32800281A>G , CM000682.2:g.32800281A>G	GRCh38
NC_000020.10:g.31388087A>G , CM000682.1:g.31388087A>G	GRCh37
NC_000020.9:g.30851748A>G	NCBI36
NG_007290.1:g.42897A>G , LRG_56:g.42897A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*839A>G	ENSP00000512497.1:n.*839A>G
ENST00000696232.1:c.1888A>G	ENSP00000512498.1:p.Asn630Asp
ENST00000696233.1:c.*631A>G	ENSP00000512499.1:n.*631A>G
ENST00000696235.1:c.*536A>G	ENSP00000512500.1:n.*536A>G
ENST00000696238.1:c.*631A>G	ENSP00000512502.1:n.*631A>G
ENST00000696239.1:c.1669A>G	ENSP00000512503.1:p.Asn557Asp
ENST00000201963.3:c.1864A>G	ENSP00000201963.3:p.Asn622Asp
ENST00000328111.6:c.1888A>G MANE Select	ENSP00000328547.2:p.Asn630Asp
ENST00000348286.6:c.1828A>G	ENSP00000337764.2:p.Asn610Asp
ENST00000353855.6:c.1828A>G	ENSP00000313397.4:p.Asn610Asp
ENST00000443239.7:c.1702A>G	ENSP00000403169.2:p.Asn568Asp
ENST00000456297.6:c.1600A>G	ENSP00000412305.1:p.Asn534Asp
NM_001207055.1:c.1702A>G	NP_001193984.1:p.Asn568Asp
NM_001207056.1:c.1600A>G	NP_001193985.1:p.Asn534Asp
NM_006892.3:c.1888A>G , LRG_56t1:c.1888A>G	NP_008823.1:p.Asn630Asp
NM_175848.1:c.1828A>G	NP_787044.1:p.Asn610Asp
NM_175849.1:c.1828A>G	NP_787045.1:p.Asn610Asp
NM_175850.2:c.1864A>G	NP_787046.1:p.Asn622Asp
XM_011528653.1:c.1864A>G	XP_011526955.1:p.Asn622Asp
XM_011528654.1:c.1738A>G	XP_011526956.1:p.Asn580Asp
XR_936510.1:n.1855A>G
XR_936511.1:n.1855A>G
XR_936512.1:n.1730A>G
XM_011528653.2:c.1864A>G	XP_011526955.1:p.Asn622Asp
XM_011528654.2:c.1738A>G	XP_011526956.1:p.Asn580Asp
XR_936510.2:n.1866A>G
XR_936511.2:n.1866A>G
XR_936512.2:n.1742A>G
NM_001207055.2:c.1702A>G	NP_001193984.1:p.Asn568Asp
NM_001207056.2:c.1600A>G	NP_001193985.1:p.Asn534Asp
NM_006892.4:c.1888A>G MANE Select	NP_008823.1:p.Asn630Asp
NM_175848.2:c.1828A>G	NP_787044.1:p.Asn610Asp
NM_175849.2:c.1828A>G	NP_787045.1:p.Asn610Asp
NM_175850.3:c.1864A>G	NP_787046.1:p.Asn622Asp