Canonical Allele Identifier: CA2091101789

Gene: RNASEH2B

Linked Data

• dbSNP Id: rs1951669469

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.50930709_50930714del , CM000675.2:g.50930709_50930714del	GRCh38
NC_000013.10:g.51504845_51504850del , CM000675.1:g.51504845_51504850del	GRCh37
NC_000013.9:g.50402846_50402851del	NCBI36
NG_009055.1:g.25954_25959del , LRG_279:g.25954_25959del

Transcript Alleles

HGVS	Amino-acid change
ENST00000336617.8:c.271_276del MANE Select	ENSP00000337623.2:p.Val91_Asp92del
ENST00000422660.6:c.271_276del	ENSP00000389877.1:p.Val91_Asp92del
ENST00000459681.3:n.69_74del
ENST00000495244.7:n.282_287del
ENST00000611510.5:c.181_186del	ENSP00000481236.3:p.Val61_Asp62del
ENST00000616907.2:c.271_276del	ENSP00000482701.2:p.Val91_Asp92del
ENST00000637648.2:c.181_186del	ENSP00000490077.2:p.Val61_Asp62del
ENST00000642207.1:c.125_130del
ENST00000642454.1:c.181_186del	ENSP00000494221.1:p.Val61_Asp62del
ENST00000642721.1:c.271_276del	ENSP00000495650.1:p.Val91_Asp92del
ENST00000642995.1:c.163_168del	ENSP00000493499.1:p.Val55_Asp56del
ENST00000643159.1:c.181_186del	ENSP00000495587.1:p.Val61_Asp62del
ENST00000643215.1:c.141_146del
ENST00000643462.1:c.*86_*91del	ENSP00000496130.1:n.*86_*91del
ENST00000643682.1:c.271_276del	ENSP00000493655.1:p.Val91_Asp92del
ENST00000643774.1:c.235_240del	ENSP00000495482.1:p.Val79_Asp80del
ENST00000644034.1:c.65-17278_65-17273del	ENSP00000495456.1:n.65-17278_65-17273del
ENST00000644183.1:c.211+1127_211+1132del	ENSP00000495657.1:n.211+1127_211+1132del
ENST00000644297.1:c.*138_*143del	ENSP00000495519.1:n.*138_*143del
ENST00000644420.1:n.297_302del
ENST00000644425.1:c.222_227del
ENST00000644518.1:c.*138_*143del	ENSP00000495793.1:n.*138_*143del
ENST00000645188.1:c.271_276del	ENSP00000496224.1:p.Val91_Asp92del
ENST00000645333.1:n.203_208del
ENST00000645370.1:c.106_111del	ENSP00000494019.1:p.Val36_Asp37del
ENST00000645549.1:n.535_540del
ENST00000645618.1:c.181_186del	ENSP00000495429.1:p.Val61_Asp62del
ENST00000645712.1:n.304_309del
ENST00000645955.1:c.271_276del	ENSP00000495755.1:p.Val91_Asp92del
ENST00000645990.1:c.271_276del	ENSP00000496571.1:p.Val91_Asp92del
ENST00000646092.1:c.235_240del	ENSP00000496293.1:p.Val79_Asp80del
ENST00000646279.1:n.568_573del
ENST00000646709.1:c.181_186del	ENSP00000495278.1:p.Val61_Asp62del
ENST00000646731.1:c.271_276del	ENSP00000493828.1:p.Val91_Asp92del
ENST00000646960.1:c.271_276del	ENSP00000496481.1:p.Val91_Asp92del
ENST00000647387.1:c.181_186del	ENSP00000495487.1:p.Val61_Asp62del
ENST00000336617.7:c.271_276del	ENSP00000337623.2:p.Val91_Asp92del
ENST00000422660.5:c.271_276del	ENSP00000389877.1:p.Val91_Asp92del
ENST00000459681.2:n.69_74del
ENST00000495244.6:n.282_287del
ENST00000611510.4:c.271_276del	ENSP00000481236.2:p.Val91_Asp92del
NM_001142279.2:c.271_276del , LRG_279t1:c.271_276del	NP_001135751.1:p.Val91_Asp92del
NM_024570.3:c.271_276del , LRG_279t2:c.271_276del	NP_078846.2:p.Val91_Asp92del
XM_005266524.2:c.271_276del	XP_005266581.1:p.Val91_Asp92del
XM_005266525.2:c.271_276del	XP_005266582.1:p.Val91_Asp92del
XM_006719867.2:c.253_258del	XP_006719930.1:p.Val85_Asp86del
XM_011535229.1:c.271_276del	XP_011533531.1:p.Val91_Asp92del
XM_011535230.1:c.271_276del	XP_011533532.1:p.Val91_Asp92del
XM_011535231.1:c.271_276del	XP_011533533.1:p.Val91_Asp92del
XM_011535232.1:c.109_114del	XP_011533534.1:p.Val37_Asp38del
XM_011535233.1:c.-343_-338del	XP_011533535.1:n.-343_-338del
XM_011535234.1:c.271_276del	XP_011533536.1:p.Val91_Asp92del
XM_006719867.4:c.253_258del	XP_006719930.1:p.Val85_Asp86del
XM_011535230.2:c.271_276del	XP_011533532.1:p.Val91_Asp92del
XM_011535231.2:c.271_276del	XP_011533533.1:p.Val91_Asp92del
XM_011535233.2:c.-343_-338del	XP_011533535.1:n.-343_-338del
XM_017020747.1:c.271_276del	XP_016876236.1:p.Val91_Asp92del
NM_024570.4:c.271_276del MANE Select	NP_078846.2:p.Val91_Asp92del