Canonical Allele Identifier: CA510210618

Gene: DNMT3B

Linked Data

• gnomAD v4: 20-32800205-T-C
• MyVariant Identifiers: chr20:g.31388011T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32800205T>C , CM000682.2:g.32800205T>C	GRCh38
NC_000020.10:g.31388011T>C , CM000682.1:g.31388011T>C	GRCh37
NC_000020.9:g.30851672T>C	NCBI36
NG_007290.1:g.42821T>C , LRG_56:g.42821T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*763T>C	ENSP00000512497.1:n.*763T>C
ENST00000696232.1:c.1812T>C	ENSP00000512498.1:p.Ser604=
ENST00000696233.1:c.*555T>C	ENSP00000512499.1:n.*555T>C
ENST00000696235.1:c.*460T>C	ENSP00000512500.1:n.*460T>C
ENST00000696238.1:c.*555T>C	ENSP00000512502.1:n.*555T>C
ENST00000696239.1:c.1593T>C	ENSP00000512503.1:p.Ser531=
ENST00000201963.3:c.1788T>C	ENSP00000201963.3:p.Ser596=
ENST00000328111.6:c.1812T>C MANE Select	ENSP00000328547.2:p.Ser604=
ENST00000348286.6:c.1752T>C	ENSP00000337764.2:p.Ser584=
ENST00000353855.6:c.1752T>C	ENSP00000313397.4:p.Ser584=
ENST00000443239.7:c.1626T>C	ENSP00000403169.2:p.Ser542=
ENST00000456297.6:c.1524T>C	ENSP00000412305.1:p.Ser508=
NM_001207055.1:c.1626T>C	NP_001193984.1:p.Ser542=
NM_001207056.1:c.1524T>C	NP_001193985.1:p.Ser508=
NM_006892.3:c.1812T>C , LRG_56t1:c.1812T>C	NP_008823.1:p.Ser604=
NM_175848.1:c.1752T>C	NP_787044.1:p.Ser584=
NM_175849.1:c.1752T>C	NP_787045.1:p.Ser584=
NM_175850.2:c.1788T>C	NP_787046.1:p.Ser596=
XM_011528653.1:c.1788T>C	XP_011526955.1:p.Ser596=
XM_011528654.1:c.1662T>C	XP_011526956.1:p.Ser554=
XR_936510.1:n.1779T>C
XR_936511.1:n.1779T>C
XR_936512.1:n.1654T>C
XM_011528653.2:c.1788T>C	XP_011526955.1:p.Ser596=
XM_011528654.2:c.1662T>C	XP_011526956.1:p.Ser554=
XR_936510.2:n.1790T>C
XR_936511.2:n.1790T>C
XR_936512.2:n.1666T>C
NM_001207055.2:c.1626T>C	NP_001193984.1:p.Ser542=
NM_001207056.2:c.1524T>C	NP_001193985.1:p.Ser508=
NM_006892.4:c.1812T>C MANE Select	NP_008823.1:p.Ser604=
NM_175848.2:c.1752T>C	NP_787044.1:p.Ser584=
NM_175849.2:c.1752T>C	NP_787045.1:p.Ser584=
NM_175850.3:c.1788T>C	NP_787046.1:p.Ser596=