Canonical Allele Identifier: CA6985525
Gene: RNASEH2B HGNC NCBI

Linked Data

ClinVar Variation Id: 645436
ClinVar RCV Id: RCV000799508
dbSNP Id: rs767086382

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50930746A>G , CM000675.2:g.50930746A>G GRCh38
NC_000013.10:g.51504882A>G , CM000675.1:g.51504882A>G GRCh37
NC_000013.9:g.50402883A>G NCBI36
NG_009055.1:g.25991A>G , LRG_279:g.25991A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000336617.8:c.308A>G MANE Select ENSP00000337623.2:p.Lys103Arg
ENST00000422660.6:c.308A>G ENSP00000389877.1:p.Lys103Arg
ENST00000459681.3:n.106A>G
ENST00000495244.7:n.319A>G
ENST00000611510.5:c.218A>G ENSP00000481236.3:p.Lys73Arg
ENST00000616907.2:c.308A>G ENSP00000482701.2:p.Lys103Arg
ENST00000637648.2:c.218A>G ENSP00000490077.2:p.Lys73Arg
ENST00000642207.1:c.162A>G
ENST00000642454.1:c.218A>G ENSP00000494221.1:p.Lys73Arg
ENST00000642721.1:c.308A>G ENSP00000495650.1:p.Lys103Arg
ENST00000642995.1:c.200A>G ENSP00000493499.1:p.Lys67Arg
ENST00000643159.1:c.218A>G ENSP00000495587.1:p.Lys73Arg
ENST00000643215.1:c.178A>G
ENST00000643462.1:c.*123A>G ENSP00000496130.1:n.*123A>G
ENST00000643682.1:c.308A>G ENSP00000493655.1:p.Lys103Arg
ENST00000643774.1:c.272A>G ENSP00000495482.1:p.Lys91Arg
ENST00000644034.1:c.65-17241A>G ENSP00000495456.1:n.65-17241A>G
ENST00000644183.1:c.211+1164A>G ENSP00000495657.1:n.211+1164A>G
ENST00000644297.1:c.*175A>G ENSP00000495519.1:n.*175A>G
ENST00000644420.1:n.334A>G
ENST00000644425.1:c.259A>G
ENST00000644518.1:c.*175A>G ENSP00000495793.1:n.*175A>G
ENST00000645188.1:c.308A>G ENSP00000496224.1:p.Lys103Arg
ENST00000645333.1:n.240A>G
ENST00000645370.1:c.143A>G ENSP00000494019.1:p.Lys48Arg
ENST00000645549.1:n.572A>G
ENST00000645618.1:c.218A>G ENSP00000495429.1:p.Lys73Arg
ENST00000645712.1:n.341A>G
ENST00000645955.1:c.308A>G ENSP00000495755.1:p.Lys103Arg
ENST00000645990.1:c.308A>G ENSP00000496571.1:p.Lys103Arg
ENST00000646092.1:c.272A>G ENSP00000496293.1:p.Lys91Arg
ENST00000646279.1:n.605A>G
ENST00000646709.1:c.218A>G ENSP00000495278.1:p.Lys73Arg
ENST00000646731.1:c.308A>G ENSP00000493828.1:p.Lys103Arg
ENST00000646960.1:c.308A>G ENSP00000496481.1:p.Lys103Arg
ENST00000647387.1:c.218A>G ENSP00000495487.1:p.Lys73Arg
ENST00000336617.7:c.308A>G ENSP00000337623.2:p.Lys103Arg
ENST00000422660.5:c.308A>G ENSP00000389877.1:p.Lys103Arg
ENST00000459681.2:n.106A>G
ENST00000495244.6:n.319A>G
ENST00000611510.4:c.308A>G ENSP00000481236.2:p.Lys103Arg
NM_001142279.2:c.308A>G , LRG_279t1:c.308A>G NP_001135751.1:p.Lys103Arg
NM_024570.3:c.308A>G , LRG_279t2:c.308A>G NP_078846.2:p.Lys103Arg
XM_005266524.2:c.308A>G XP_005266581.1:p.Lys103Arg
XM_005266525.2:c.308A>G XP_005266582.1:p.Lys103Arg
XM_006719867.2:c.290A>G XP_006719930.1:p.Lys97Arg
XM_011535229.1:c.308A>G XP_011533531.1:p.Lys103Arg
XM_011535230.1:c.308A>G XP_011533532.1:p.Lys103Arg
XM_011535231.1:c.308A>G XP_011533533.1:p.Lys103Arg
XM_011535232.1:c.146A>G XP_011533534.1:p.Lys49Arg
XM_011535233.1:c.-306A>G XP_011533535.1:n.-306A>G
XM_011535234.1:c.308A>G XP_011533536.1:p.Lys103Arg
XM_006719867.4:c.290A>G XP_006719930.1:p.Lys97Arg
XM_011535230.2:c.308A>G XP_011533532.1:p.Lys103Arg
XM_011535231.2:c.308A>G XP_011533533.1:p.Lys103Arg
XM_011535233.2:c.-306A>G XP_011533535.1:n.-306A>G
XM_017020747.1:c.308A>G XP_016876236.1:p.Lys103Arg
NM_024570.4:c.308A>G MANE Select NP_078846.2:p.Lys103Arg