Canonical Allele Identifier: CA16619813
Gene: RNASEH2B HGNC NCBI

Linked Data

ClinVar Variation Id: 424565
ClinVar RCV Id: RCV000486862
dbSNP Id: rs1064797046

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50948073G>A , CM000675.2:g.50948073G>A GRCh38
NC_000013.10:g.51522209G>A , CM000675.1:g.51522209G>A GRCh37
NC_000013.9:g.50420210G>A NCBI36
NG_009055.1:g.43318G>A , LRG_279:g.43318G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000336617.8:c.698+5G>A MANE Select ENSP00000337623.2:n.698+5G>A
ENST00000422660.6:c.698+5G>A ENSP00000389877.1:n.698+5G>A
ENST00000459681.3:n.381+5G>A
ENST00000465541.2:n.5+5G>A
ENST00000495244.7:n.709+5G>A
ENST00000611510.5:c.608+5G>A ENSP00000481236.3:n.608+5G>A
ENST00000616907.2:c.698+5G>A ENSP00000482701.2:n.698+5G>A
ENST00000642207.1:c.437+5G>A
ENST00000642454.1:c.608+5G>A ENSP00000494221.1:n.608+5G>A
ENST00000642721.1:c.698+5G>A ENSP00000495650.1:n.698+5G>A
ENST00000642995.1:c.581+5G>A ENSP00000493499.1:n.581+5G>A
ENST00000643159.1:c.608+5G>A ENSP00000495587.1:n.608+5G>A
ENST00000643215.1:c.568+5G>A
ENST00000643405.1:c.346+5G>A
ENST00000643529.1:c.211+5G>A
ENST00000643682.1:c.698+5G>A ENSP00000493655.1:n.698+5G>A
ENST00000643774.1:c.662+5G>A ENSP00000495482.1:n.662+5G>A
ENST00000644034.1:c.146+5G>A ENSP00000495456.1:n.146+5G>A
ENST00000644183.1:c.588+5G>A ENSP00000495657.1:n.588+5G>A
ENST00000644297.1:c.*556+5G>A ENSP00000495519.1:n.*556+5G>A
ENST00000644420.1:n.724+5G>A
ENST00000644425.1:c.649+5G>A
ENST00000644518.1:c.*565+5G>A ENSP00000495793.1:n.*565+5G>A
ENST00000645188.1:c.689+5G>A ENSP00000496224.1:n.689+5G>A
ENST00000645201.1:n.95+5G>A
ENST00000645333.1:n.635G>A
ENST00000645370.1:c.533+5G>A ENSP00000494019.1:n.533+5G>A
ENST00000645618.1:c.608+5G>A ENSP00000495429.1:n.608+5G>A
ENST00000645712.1:n.722+5G>A
ENST00000645912.1:c.36+5G>A
ENST00000645955.1:c.698+5G>A ENSP00000495755.1:n.698+5G>A
ENST00000645990.1:c.698+5G>A ENSP00000496571.1:n.698+5G>A
ENST00000646092.1:c.662+5G>A ENSP00000496293.1:n.662+5G>A
ENST00000646279.1:n.995+5G>A
ENST00000646339.1:c.360+5G>A ENSP00000495773.1:n.360+5G>A
ENST00000646709.1:c.608+5G>A ENSP00000495278.1:n.608+5G>A
ENST00000646731.1:c.689+5G>A ENSP00000493828.1:n.689+5G>A
ENST00000646960.1:c.698+5G>A ENSP00000496481.1:n.698+5G>A
ENST00000646964.1:n.1337+5G>A
ENST00000647387.1:c.608+5G>A ENSP00000495487.1:n.608+5G>A
ENST00000336617.7:c.698+5G>A ENSP00000337623.2:n.698+5G>A
ENST00000422660.5:c.698+5G>A ENSP00000389877.1:n.698+5G>A
ENST00000495244.6:n.709+5G>A
ENST00000611510.4:c.698+5G>A ENSP00000481236.2:n.698+5G>A
ENST00000613449.4:n.2760+5G>A
ENST00000616907.1:c.81+5G>A
ENST00000621641.1:n.286+5G>A
NM_001142279.2:c.698+5G>A , LRG_279t1:c.698+5G>A NP_001135751.1:n.698+5G>A
NM_024570.3:c.698+5G>A , LRG_279t2:c.698+5G>A NP_078846.2:n.698+5G>A
XM_005266524.2:c.698+5G>A XP_005266581.1:n.698+5G>A
XM_005266525.2:c.698+5G>A XP_005266582.1:n.698+5G>A
XM_006719867.2:c.680+5G>A XP_006719930.1:n.680+5G>A
XM_011535229.1:c.698+5G>A XP_011533531.1:n.698+5G>A
XM_011535230.1:c.698+5G>A XP_011533532.1:n.698+5G>A
XM_011535231.1:c.698+5G>A XP_011533533.1:n.698+5G>A
XM_011535232.1:c.536+5G>A XP_011533534.1:n.536+5G>A
XM_011535233.1:c.290+5G>A XP_011533535.1:n.290+5G>A
XM_006719867.4:c.680+5G>A XP_006719930.1:n.680+5G>A
XM_011535230.2:c.698+5G>A XP_011533532.1:n.698+5G>A
XM_011535231.2:c.698+5G>A XP_011533533.1:n.698+5G>A
XM_011535233.2:c.290+5G>A XP_011533535.1:n.290+5G>A
XM_017020747.1:c.698+5G>A XP_016876236.1:n.698+5G>A
NM_024570.4:c.698+5G>A MANE Select NP_078846.2:n.698+5G>A