Canonical Allele Identifier: CA510210667

Gene: DNMT3B

Linked Data

• MyVariant Identifiers: chr20:g.31388089C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32800283C>T , CM000682.2:g.32800283C>T	GRCh38
NC_000020.10:g.31388089C>T , CM000682.1:g.31388089C>T	GRCh37
NC_000020.9:g.30851750C>T	NCBI36
NG_007290.1:g.42899C>T , LRG_56:g.42899C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*841C>T	ENSP00000512497.1:n.*841C>T
ENST00000696232.1:c.1890C>T	ENSP00000512498.1:p.Asn630=
ENST00000696233.1:c.*633C>T	ENSP00000512499.1:n.*633C>T
ENST00000696235.1:c.*538C>T	ENSP00000512500.1:n.*538C>T
ENST00000696238.1:c.*633C>T	ENSP00000512502.1:n.*633C>T
ENST00000696239.1:c.1671C>T	ENSP00000512503.1:p.Asn557=
ENST00000201963.3:c.1866C>T	ENSP00000201963.3:p.Asn622=
ENST00000328111.6:c.1890C>T MANE Select	ENSP00000328547.2:p.Asn630=
ENST00000348286.6:c.1830C>T	ENSP00000337764.2:p.Asn610=
ENST00000353855.6:c.1830C>T	ENSP00000313397.4:p.Asn610=
ENST00000443239.7:c.1704C>T	ENSP00000403169.2:p.Asn568=
ENST00000456297.6:c.1602C>T	ENSP00000412305.1:p.Asn534=
NM_001207055.1:c.1704C>T	NP_001193984.1:p.Asn568=
NM_001207056.1:c.1602C>T	NP_001193985.1:p.Asn534=
NM_006892.3:c.1890C>T , LRG_56t1:c.1890C>T	NP_008823.1:p.Asn630=
NM_175848.1:c.1830C>T	NP_787044.1:p.Asn610=
NM_175849.1:c.1830C>T	NP_787045.1:p.Asn610=
NM_175850.2:c.1866C>T	NP_787046.1:p.Asn622=
XM_011528653.1:c.1866C>T	XP_011526955.1:p.Asn622=
XM_011528654.1:c.1740C>T	XP_011526956.1:p.Asn580=
XR_936510.1:n.1857C>T
XR_936511.1:n.1857C>T
XR_936512.1:n.1732C>T
XM_011528653.2:c.1866C>T	XP_011526955.1:p.Asn622=
XM_011528654.2:c.1740C>T	XP_011526956.1:p.Asn580=
XR_936510.2:n.1868C>T
XR_936511.2:n.1868C>T
XR_936512.2:n.1744C>T
NM_001207055.2:c.1704C>T	NP_001193984.1:p.Asn568=
NM_001207056.2:c.1602C>T	NP_001193985.1:p.Asn534=
NM_006892.4:c.1890C>T MANE Select	NP_008823.1:p.Asn630=
NM_175848.2:c.1830C>T	NP_787044.1:p.Asn610=
NM_175849.2:c.1830C>T	NP_787045.1:p.Asn610=
NM_175850.3:c.1866C>T	NP_787046.1:p.Asn622=