Canonical Allele Identifier: CA2623068095

Gene: RNASEH2B

Linked Data

• gnomAD v4: 13-50948195-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.50948195A>G , CM000675.2:g.50948195A>G	GRCh38
NC_000013.10:g.51522331A>G , CM000675.1:g.51522331A>G	GRCh37
NC_000013.9:g.50420332A>G	NCBI36
NG_009055.1:g.43440A>G , LRG_279:g.43440A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336617.8:c.698+127A>G MANE Select	ENSP00000337623.2:n.698+127A>G
ENST00000422660.6:c.698+127A>G	ENSP00000389877.1:n.698+127A>G
ENST00000459681.3:n.381+127A>G
ENST00000465541.2:n.5+127A>G
ENST00000495244.7:n.709+127A>G
ENST00000611510.5:c.608+127A>G	ENSP00000481236.3:n.608+127A>G
ENST00000616907.2:c.698+127A>G	ENSP00000482701.2:n.698+127A>G
ENST00000642207.1:c.437+127A>G
ENST00000642454.1:c.608+127A>G	ENSP00000494221.1:n.608+127A>G
ENST00000642721.1:c.698+127A>G	ENSP00000495650.1:n.698+127A>G
ENST00000642995.1:c.581+127A>G	ENSP00000493499.1:n.581+127A>G
ENST00000643159.1:c.608+127A>G	ENSP00000495587.1:n.608+127A>G
ENST00000643215.1:c.568+127A>G
ENST00000643405.1:c.346+127A>G
ENST00000643529.1:c.211+127A>G
ENST00000643682.1:c.698+127A>G	ENSP00000493655.1:n.698+127A>G
ENST00000643774.1:c.662+127A>G	ENSP00000495482.1:n.662+127A>G
ENST00000644034.1:c.146+127A>G	ENSP00000495456.1:n.146+127A>G
ENST00000644183.1:c.588+127A>G	ENSP00000495657.1:n.588+127A>G
ENST00000644297.1:c.*556+127A>G	ENSP00000495519.1:n.*556+127A>G
ENST00000644420.1:n.724+127A>G
ENST00000644425.1:c.649+127A>G
ENST00000644518.1:c.*565+127A>G	ENSP00000495793.1:n.*565+127A>G
ENST00000645188.1:c.689+127A>G	ENSP00000496224.1:n.689+127A>G
ENST00000645201.1:n.95+127A>G
ENST00000645333.1:n.757A>G
ENST00000645370.1:c.533+127A>G	ENSP00000494019.1:n.533+127A>G
ENST00000645618.1:c.608+127A>G	ENSP00000495429.1:n.608+127A>G
ENST00000645712.1:n.722+127A>G
ENST00000645912.1:c.36+127A>G
ENST00000645955.1:c.698+127A>G	ENSP00000495755.1:n.698+127A>G
ENST00000645990.1:c.698+127A>G	ENSP00000496571.1:n.698+127A>G
ENST00000646092.1:c.662+127A>G	ENSP00000496293.1:n.662+127A>G
ENST00000646279.1:n.995+127A>G
ENST00000646339.1:c.360+127A>G	ENSP00000495773.1:n.360+127A>G
ENST00000646709.1:c.608+127A>G	ENSP00000495278.1:n.608+127A>G
ENST00000646731.1:c.689+127A>G	ENSP00000493828.1:n.689+127A>G
ENST00000646960.1:c.698+127A>G	ENSP00000496481.1:n.698+127A>G
ENST00000646964.1:n.1337+127A>G
ENST00000647387.1:c.608+127A>G	ENSP00000495487.1:n.608+127A>G
ENST00000336617.7:c.698+127A>G	ENSP00000337623.2:n.698+127A>G
ENST00000422660.5:c.698+127A>G	ENSP00000389877.1:n.698+127A>G
ENST00000495244.6:n.709+127A>G
ENST00000611510.4:c.698+127A>G	ENSP00000481236.2:n.698+127A>G
ENST00000613449.4:n.2760+127A>G
ENST00000616907.1:c.81+127A>G
ENST00000621641.1:n.286+127A>G
NM_001142279.2:c.698+127A>G , LRG_279t1:c.698+127A>G	NP_001135751.1:n.698+127A>G
NM_024570.3:c.698+127A>G , LRG_279t2:c.698+127A>G	NP_078846.2:n.698+127A>G
XM_005266524.2:c.698+127A>G	XP_005266581.1:n.698+127A>G
XM_005266525.2:c.698+127A>G	XP_005266582.1:n.698+127A>G
XM_006719867.2:c.680+127A>G	XP_006719930.1:n.680+127A>G
XM_011535229.1:c.698+127A>G	XP_011533531.1:n.698+127A>G
XM_011535230.1:c.698+127A>G	XP_011533532.1:n.698+127A>G
XM_011535231.1:c.698+127A>G	XP_011533533.1:n.698+127A>G
XM_011535232.1:c.536+127A>G	XP_011533534.1:n.536+127A>G
XM_011535233.1:c.290+127A>G	XP_011533535.1:n.290+127A>G
XM_006719867.4:c.680+127A>G	XP_006719930.1:n.680+127A>G
XM_011535230.2:c.698+127A>G	XP_011533532.1:n.698+127A>G
XM_011535231.2:c.698+127A>G	XP_011533533.1:n.698+127A>G
XM_011535233.2:c.290+127A>G	XP_011533535.1:n.290+127A>G
XM_017020747.1:c.698+127A>G	XP_016876236.1:n.698+127A>G
NM_024570.4:c.698+127A>G MANE Select	NP_078846.2:n.698+127A>G