Canonical Allele Identifier: CA2623044861
Gene: RNASEH2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50930797_50930798insAAAATAGTT , CM000675.2:g.50930797_50930798insAAAATAGTT GRCh38
NC_000013.10:g.51504933_51504934insAAAATAGTT , CM000675.1:g.51504933_51504934insAAAATAGTT GRCh37
NC_000013.9:g.50402934_50402935insAAAATAGTT NCBI36
NG_009055.1:g.26042_26043insAAAATAGTT , LRG_279:g.26042_26043insAAAATAGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000336617.8:c.321+38_321+39insAAAATAGTT MANE Select ENSP00000337623.2:n.321+38_321+39insAAAATAGTT
ENST00000422660.6:c.321+38_321+39insAAAATAGTT ENSP00000389877.1:n.321+38_321+39insAAAATAGTT
ENST00000459681.3:n.119+38_119+39insAAAATAGTT
ENST00000495244.7:n.332+38_332+39insAAAATAGTT
ENST00000611510.5:c.231+38_231+39insAAAATAGTT ENSP00000481236.3:n.231+38_231+39insAAAATAGTT
ENST00000616907.2:c.321+38_321+39insAAAATAGTT ENSP00000482701.2:n.321+38_321+39insAAAATAGTT
ENST00000637648.2:c.231+38_231+39insAAAATAGTT ENSP00000490077.2:n.231+38_231+39insAAAATAGTT
ENST00000642207.1:c.175+38_175+39insAAAATAGTT
ENST00000642454.1:c.231+38_231+39insAAAATAGTT ENSP00000494221.1:n.231+38_231+39insAAAATAGTT
ENST00000642721.1:c.321+38_321+39insAAAATAGTT ENSP00000495650.1:n.321+38_321+39insAAAATAGTT
ENST00000642995.1:c.213+38_213+39insAAAATAGTT ENSP00000493499.1:n.213+38_213+39insAAAATAGTT
ENST00000643159.1:c.231+38_231+39insAAAATAGTT ENSP00000495587.1:n.231+38_231+39insAAAATAGTT
ENST00000643215.1:c.191+38_191+39insAAAATAGTT
ENST00000643462.1:c.*136+38_*136+39insAAAATAGTT ENSP00000496130.1:n.*136+38_*136+39insAAAATAGTT
ENST00000643682.1:c.321+38_321+39insAAAATAGTT ENSP00000493655.1:n.321+38_321+39insAAAATAGTT
ENST00000643774.1:c.285+38_285+39insAAAATAGTT ENSP00000495482.1:n.285+38_285+39insAAAATAGTT
ENST00000644034.1:c.65-17190_65-17189insAAAATAGTT ENSP00000495456.1:n.65-17190_65-17189insAAAATAGTT
ENST00000644183.1:c.211+1215_211+1216insAAAATAGTT ENSP00000495657.1:n.211+1215_211+1216insAAAATAGTT
ENST00000644297.1:c.*188+38_*188+39insAAAATAGTT ENSP00000495519.1:n.*188+38_*188+39insAAAATAGTT
ENST00000644420.1:n.347+38_347+39insAAAATAGTT
ENST00000644425.1:c.272+38_272+39insAAAATAGTT
ENST00000644518.1:c.*188+38_*188+39insAAAATAGTT ENSP00000495793.1:n.*188+38_*188+39insAAAATAGTT
ENST00000645188.1:c.321+38_321+39insAAAATAGTT ENSP00000496224.1:n.321+38_321+39insAAAATAGTT
ENST00000645333.1:n.253+38_253+39insAAAATAGTT
ENST00000645370.1:c.156+38_156+39insAAAATAGTT ENSP00000494019.1:n.156+38_156+39insAAAATAGTT
ENST00000645549.1:n.585+38_585+39insAAAATAGTT
ENST00000645618.1:c.231+38_231+39insAAAATAGTT ENSP00000495429.1:n.231+38_231+39insAAAATAGTT
ENST00000645712.1:n.354+38_354+39insAAAATAGTT
ENST00000645955.1:c.321+38_321+39insAAAATAGTT ENSP00000495755.1:n.321+38_321+39insAAAATAGTT
ENST00000645990.1:c.321+38_321+39insAAAATAGTT ENSP00000496571.1:n.321+38_321+39insAAAATAGTT
ENST00000646092.1:c.285+38_285+39insAAAATAGTT ENSP00000496293.1:n.285+38_285+39insAAAATAGTT
ENST00000646279.1:n.618+38_618+39insAAAATAGTT
ENST00000646339.1:c.47_48insAAAATAGTT ENSP00000495773.1:p.Gln17LysfsTer2
ENST00000646709.1:c.231+38_231+39insAAAATAGTT ENSP00000495278.1:n.231+38_231+39insAAAATAGTT
ENST00000646731.1:c.321+38_321+39insAAAATAGTT ENSP00000493828.1:n.321+38_321+39insAAAATAGTT
ENST00000646960.1:c.321+38_321+39insAAAATAGTT ENSP00000496481.1:n.321+38_321+39insAAAATAGTT
ENST00000647387.1:c.231+38_231+39insAAAATAGTT ENSP00000495487.1:n.231+38_231+39insAAAATAGTT
ENST00000336617.7:c.321+38_321+39insAAAATAGTT ENSP00000337623.2:n.321+38_321+39insAAAATAGTT
ENST00000422660.5:c.321+38_321+39insAAAATAGTT ENSP00000389877.1:n.321+38_321+39insAAAATAGTT
ENST00000495244.6:n.332+38_332+39insAAAATAGTT
ENST00000611510.4:c.321+38_321+39insAAAATAGTT ENSP00000481236.2:n.321+38_321+39insAAAATAGTT
NM_001142279.2:c.321+38_321+39insAAAATAGTT , LRG_279t1:c.321+38_321+39insAAAATAGTT NP_001135751.1:n.321+38_321+39insAAAATAGTT
NM_024570.3:c.321+38_321+39insAAAATAGTT , LRG_279t2:c.321+38_321+39insAAAATAGTT NP_078846.2:n.321+38_321+39insAAAATAGTT
XM_005266524.2:c.321+38_321+39insAAAATAGTT XP_005266581.1:n.321+38_321+39insAAAATAGTT
XM_005266525.2:c.321+38_321+39insAAAATAGTT XP_005266582.1:n.321+38_321+39insAAAATAGTT
XM_006719867.2:c.303+38_303+39insAAAATAGTT XP_006719930.1:n.303+38_303+39insAAAATAGTT
XM_011535229.1:c.321+38_321+39insAAAATAGTT XP_011533531.1:n.321+38_321+39insAAAATAGTT
XM_011535230.1:c.321+38_321+39insAAAATAGTT XP_011533532.1:n.321+38_321+39insAAAATAGTT
XM_011535231.1:c.321+38_321+39insAAAATAGTT XP_011533533.1:n.321+38_321+39insAAAATAGTT
XM_011535232.1:c.159+38_159+39insAAAATAGTT XP_011533534.1:n.159+38_159+39insAAAATAGTT
XM_011535233.1:c.-293+38_-293+39insAAAATAGTT XP_011533535.1:n.-293+38_-293+39insAAAATAGTT
XM_011535234.1:c.321+38_321+39insAAAATAGTT XP_011533536.1:n.321+38_321+39insAAAATAGTT
XM_006719867.4:c.303+38_303+39insAAAATAGTT XP_006719930.1:n.303+38_303+39insAAAATAGTT
XM_011535230.2:c.321+38_321+39insAAAATAGTT XP_011533532.1:n.321+38_321+39insAAAATAGTT
XM_011535231.2:c.321+38_321+39insAAAATAGTT XP_011533533.1:n.321+38_321+39insAAAATAGTT
XM_011535233.2:c.-293+38_-293+39insAAAATAGTT XP_011533535.1:n.-293+38_-293+39insAAAATAGTT
XM_017020747.1:c.321+38_321+39insAAAATAGTT XP_016876236.1:n.321+38_321+39insAAAATAGTT
NM_024570.4:c.321+38_321+39insAAAATAGTT MANE Select NP_078846.2:n.321+38_321+39insAAAATAGTT