Canonical Allele Identifier: CA6985516
Gene: RNASEH2B HGNC NCBI

Linked Data

dbSNP Id: rs777149786

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50930701C>G , CM000675.2:g.50930701C>G GRCh38
NC_000013.10:g.51504837C>G , CM000675.1:g.51504837C>G GRCh37
NC_000013.9:g.50402838C>G NCBI36
NG_009055.1:g.25946C>G , LRG_279:g.25946C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000336617.8:c.263C>G MANE Select ENSP00000337623.2:p.Ala88Gly
ENST00000422660.6:c.263C>G ENSP00000389877.1:p.Ala88Gly
ENST00000459681.3:n.61C>G
ENST00000495244.7:n.274C>G
ENST00000611510.5:c.173C>G ENSP00000481236.3:p.Ala58Gly
ENST00000616907.2:c.263C>G ENSP00000482701.2:p.Ala88Gly
ENST00000637648.2:c.173C>G ENSP00000490077.2:p.Ala58Gly
ENST00000642207.1:c.117C>G
ENST00000642454.1:c.173C>G ENSP00000494221.1:p.Ala58Gly
ENST00000642721.1:c.263C>G ENSP00000495650.1:p.Ala88Gly
ENST00000642995.1:c.155C>G ENSP00000493499.1:p.Ala52Gly
ENST00000643159.1:c.173C>G ENSP00000495587.1:p.Ala58Gly
ENST00000643215.1:c.133C>G
ENST00000643462.1:c.*78C>G ENSP00000496130.1:n.*78C>G
ENST00000643682.1:c.263C>G ENSP00000493655.1:p.Ala88Gly
ENST00000643774.1:c.227C>G ENSP00000495482.1:p.Ala76Gly
ENST00000644034.1:c.65-17286C>G ENSP00000495456.1:n.65-17286C>G
ENST00000644183.1:c.211+1119C>G ENSP00000495657.1:n.211+1119C>G
ENST00000644297.1:c.*130C>G ENSP00000495519.1:n.*130C>G
ENST00000644420.1:n.289C>G
ENST00000644425.1:c.214C>G
ENST00000644518.1:c.*130C>G ENSP00000495793.1:n.*130C>G
ENST00000645188.1:c.263C>G ENSP00000496224.1:p.Ala88Gly
ENST00000645333.1:n.195C>G
ENST00000645370.1:c.98C>G ENSP00000494019.1:p.Ala33Gly
ENST00000645549.1:n.527C>G
ENST00000645618.1:c.173C>G ENSP00000495429.1:p.Ala58Gly
ENST00000645712.1:n.296C>G
ENST00000645955.1:c.263C>G ENSP00000495755.1:p.Ala88Gly
ENST00000645990.1:c.263C>G ENSP00000496571.1:p.Ala88Gly
ENST00000646092.1:c.227C>G ENSP00000496293.1:p.Ala76Gly
ENST00000646279.1:n.560C>G
ENST00000646709.1:c.173C>G ENSP00000495278.1:p.Ala58Gly
ENST00000646731.1:c.263C>G ENSP00000493828.1:p.Ala88Gly
ENST00000646960.1:c.263C>G ENSP00000496481.1:p.Ala88Gly
ENST00000647387.1:c.173C>G ENSP00000495487.1:p.Ala58Gly
ENST00000336617.7:c.263C>G ENSP00000337623.2:p.Ala88Gly
ENST00000422660.5:c.263C>G ENSP00000389877.1:p.Ala88Gly
ENST00000459681.2:n.61C>G
ENST00000495244.6:n.274C>G
ENST00000611510.4:c.263C>G ENSP00000481236.2:p.Ala88Gly
NM_001142279.2:c.263C>G , LRG_279t1:c.263C>G NP_001135751.1:p.Ala88Gly
NM_024570.3:c.263C>G , LRG_279t2:c.263C>G NP_078846.2:p.Ala88Gly
XM_005266524.2:c.263C>G XP_005266581.1:p.Ala88Gly
XM_005266525.2:c.263C>G XP_005266582.1:p.Ala88Gly
XM_006719867.2:c.245C>G XP_006719930.1:p.Ala82Gly
XM_011535229.1:c.263C>G XP_011533531.1:p.Ala88Gly
XM_011535230.1:c.263C>G XP_011533532.1:p.Ala88Gly
XM_011535231.1:c.263C>G XP_011533533.1:p.Ala88Gly
XM_011535232.1:c.101C>G XP_011533534.1:p.Ala34Gly
XM_011535233.1:c.-351C>G XP_011533535.1:n.-351C>G
XM_011535234.1:c.263C>G XP_011533536.1:p.Ala88Gly
XM_006719867.4:c.245C>G XP_006719930.1:p.Ala82Gly
XM_011535230.2:c.263C>G XP_011533532.1:p.Ala88Gly
XM_011535231.2:c.263C>G XP_011533533.1:p.Ala88Gly
XM_011535233.2:c.-351C>G XP_011533535.1:n.-351C>G
XM_017020747.1:c.263C>G XP_016876236.1:p.Ala88Gly
NM_024570.4:c.263C>G MANE Select NP_078846.2:p.Ala88Gly