Canonical Allele Identifier: CA388259902

Gene: RNASEH2B

Linked Data

• MyVariant Identifiers: chr13:g.51522184T>G (hg19) ; chr13:g.50948048T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.50948048T>G , CM000675.2:g.50948048T>G	GRCh38
NC_000013.10:g.51522184T>G , CM000675.1:g.51522184T>G	GRCh37
NC_000013.9:g.50420185T>G	NCBI36
NG_009055.1:g.43293T>G , LRG_279:g.43293T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336617.8:c.678T>G MANE Select	ENSP00000337623.2:p.Asp226Glu
ENST00000422660.6:c.678T>G	ENSP00000389877.1:p.Asp226Glu
ENST00000459681.3:n.361T>G
ENST00000495244.7:n.689T>G
ENST00000611510.5:c.588T>G	ENSP00000481236.3:p.Asp196Glu
ENST00000616907.2:c.678T>G	ENSP00000482701.2:p.Asp226Glu
ENST00000642207.1:c.417T>G
ENST00000642454.1:c.588T>G	ENSP00000494221.1:p.Asp196Glu
ENST00000642721.1:c.678T>G	ENSP00000495650.1:p.Asp226Glu
ENST00000642995.1:c.561T>G	ENSP00000493499.1:p.Asp187Glu
ENST00000643159.1:c.588T>G	ENSP00000495587.1:p.Asp196Glu
ENST00000643215.1:c.548T>G
ENST00000643405.1:c.326T>G
ENST00000643529.1:c.191T>G
ENST00000643682.1:c.678T>G	ENSP00000493655.1:p.Asp226Glu
ENST00000643774.1:c.642T>G	ENSP00000495482.1:p.Asp214Glu
ENST00000644034.1:c.126T>G	ENSP00000495456.1:p.Asp42Glu
ENST00000644183.1:c.568T>G	ENSP00000495657.1:n.568T>G
ENST00000644297.1:c.*536T>G	ENSP00000495519.1:n.*536T>G
ENST00000644420.1:n.704T>G
ENST00000644425.1:c.629T>G
ENST00000644518.1:c.*545T>G	ENSP00000495793.1:n.*545T>G
ENST00000645188.1:c.669T>G	ENSP00000496224.1:p.Asp223Glu
ENST00000645201.1:n.75T>G
ENST00000645333.1:n.610T>G
ENST00000645370.1:c.513T>G	ENSP00000494019.1:p.Asp171Glu
ENST00000645618.1:c.588T>G	ENSP00000495429.1:p.Asp196Glu
ENST00000645712.1:n.702T>G
ENST00000645912.1:c.16T>G
ENST00000645955.1:c.678T>G	ENSP00000495755.1:p.Asp226Glu
ENST00000645990.1:c.678T>G	ENSP00000496571.1:p.Asp226Glu
ENST00000646092.1:c.642T>G	ENSP00000496293.1:p.Asp214Glu
ENST00000646279.1:n.975T>G
ENST00000646339.1:c.340T>G	ENSP00000495773.1:n.340T>G
ENST00000646709.1:c.588T>G	ENSP00000495278.1:p.Asp196Glu
ENST00000646731.1:c.669T>G	ENSP00000493828.1:p.Asp223Glu
ENST00000646960.1:c.678T>G	ENSP00000496481.1:p.Asp226Glu
ENST00000646964.1:n.1317T>G
ENST00000647387.1:c.588T>G	ENSP00000495487.1:p.Asp196Glu
ENST00000336617.7:c.678T>G	ENSP00000337623.2:p.Asp226Glu
ENST00000422660.5:c.678T>G	ENSP00000389877.1:p.Asp226Glu
ENST00000495244.6:n.689T>G
ENST00000611510.4:c.678T>G	ENSP00000481236.2:p.Asp226Glu
ENST00000613449.4:n.2740T>G
ENST00000616907.1:c.61T>G
ENST00000621641.1:n.266T>G
NM_001142279.2:c.678T>G , LRG_279t1:c.678T>G	NP_001135751.1:p.Asp226Glu
NM_024570.3:c.678T>G , LRG_279t2:c.678T>G	NP_078846.2:p.Asp226Glu
XM_005266524.2:c.678T>G	XP_005266581.1:p.Asp226Glu
XM_005266525.2:c.678T>G	XP_005266582.1:p.Asp226Glu
XM_006719867.2:c.660T>G	XP_006719930.1:p.Asp220Glu
XM_011535229.1:c.678T>G	XP_011533531.1:p.Asp226Glu
XM_011535230.1:c.678T>G	XP_011533532.1:p.Asp226Glu
XM_011535231.1:c.678T>G	XP_011533533.1:p.Asp226Glu
XM_011535232.1:c.516T>G	XP_011533534.1:p.Asp172Glu
XM_011535233.1:c.270T>G	XP_011533535.1:p.Asp90Glu
XM_006719867.4:c.660T>G	XP_006719930.1:p.Asp220Glu
XM_011535230.2:c.678T>G	XP_011533532.1:p.Asp226Glu
XM_011535231.2:c.678T>G	XP_011533533.1:p.Asp226Glu
XM_011535233.2:c.270T>G	XP_011533535.1:p.Asp90Glu
XM_017020747.1:c.678T>G	XP_016876236.1:p.Asp226Glu
NM_024570.4:c.678T>G MANE Select	NP_078846.2:p.Asp226Glu