Canonical Allele Identifier: CA2623068022

Gene: RNASEH2B

Linked Data

• gnomAD v4: 13-50947962-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.50947964_50947965del , CM000675.2:g.50947964_50947965del	GRCh38
NC_000013.10:g.51522100_51522101del , CM000675.1:g.51522100_51522101del	GRCh37
NC_000013.9:g.50420101_50420102del	NCBI36
NG_009055.1:g.43209_43210del , LRG_279:g.43209_43210del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336617.8:c.617-23_617-22del MANE Select	ENSP00000337623.2:n.617-23_617-22del
ENST00000422660.6:c.617-23_617-22del	ENSP00000389877.1:n.617-23_617-22del
ENST00000459681.3:n.300-23_300-22del
ENST00000495244.7:n.628-23_628-22del
ENST00000611510.5:c.527-23_527-22del	ENSP00000481236.3:n.527-23_527-22del
ENST00000616907.2:c.617-23_617-22del	ENSP00000482701.2:n.617-23_617-22del
ENST00000642207.1:c.356-23_356-22del
ENST00000642454.1:c.527-23_527-22del	ENSP00000494221.1:n.527-23_527-22del
ENST00000642721.1:c.617-23_617-22del	ENSP00000495650.1:n.617-23_617-22del
ENST00000642995.1:c.500-23_500-22del	ENSP00000493499.1:n.500-23_500-22del
ENST00000643159.1:c.527-23_527-22del	ENSP00000495587.1:n.527-23_527-22del
ENST00000643215.1:c.487-23_487-22del
ENST00000643405.1:c.265-23_265-22del
ENST00000643529.1:c.130-23_130-22del
ENST00000643682.1:c.617-23_617-22del	ENSP00000493655.1:n.617-23_617-22del
ENST00000643774.1:c.581-23_581-22del	ENSP00000495482.1:n.581-23_581-22del
ENST00000644034.1:c.65-23_65-22del	ENSP00000495456.1:n.65-23_65-22del
ENST00000644183.1:c.507-23_507-22del	ENSP00000495657.1:n.507-23_507-22del
ENST00000644297.1:c.*475-23_*475-22del	ENSP00000495519.1:n.*475-23_*475-22del
ENST00000644420.1:n.643-23_643-22del
ENST00000644425.1:c.568-23_568-22del
ENST00000644518.1:c.*484-23_*484-22del	ENSP00000495793.1:n.*484-23_*484-22del
ENST00000645188.1:c.608-23_608-22del	ENSP00000496224.1:n.608-23_608-22del
ENST00000645201.1:n.14-23_14-22del
ENST00000645333.1:n.549-23_549-22del
ENST00000645370.1:c.452-23_452-22del	ENSP00000494019.1:n.452-23_452-22del
ENST00000645618.1:c.527-23_527-22del	ENSP00000495429.1:n.527-23_527-22del
ENST00000645712.1:n.641-23_641-22del
ENST00000645955.1:c.617-23_617-22del	ENSP00000495755.1:n.617-23_617-22del
ENST00000645990.1:c.617-23_617-22del	ENSP00000496571.1:n.617-23_617-22del
ENST00000646092.1:c.581-23_581-22del	ENSP00000496293.1:n.581-23_581-22del
ENST00000646279.1:n.914-23_914-22del
ENST00000646339.1:c.279-23_279-22del	ENSP00000495773.1:n.279-23_279-22del
ENST00000646709.1:c.527-23_527-22del	ENSP00000495278.1:n.527-23_527-22del
ENST00000646731.1:c.608-23_608-22del	ENSP00000493828.1:n.608-23_608-22del
ENST00000646960.1:c.617-23_617-22del	ENSP00000496481.1:n.617-23_617-22del
ENST00000646964.1:n.1256-23_1256-22del
ENST00000647387.1:c.527-23_527-22del	ENSP00000495487.1:n.527-23_527-22del
ENST00000336617.7:c.617-23_617-22del	ENSP00000337623.2:n.617-23_617-22del
ENST00000422660.5:c.617-23_617-22del	ENSP00000389877.1:n.617-23_617-22del
ENST00000495244.6:n.628-23_628-22del
ENST00000611510.4:c.617-23_617-22del	ENSP00000481236.2:n.617-23_617-22del
ENST00000613449.4:n.2679-23_2679-22del
ENST00000621641.1:n.205-23_205-22del
NM_001142279.2:c.617-23_617-22del , LRG_279t1:c.617-23_617-22del	NP_001135751.1:n.617-23_617-22del
NM_024570.3:c.617-23_617-22del , LRG_279t2:c.617-23_617-22del	NP_078846.2:n.617-23_617-22del
XM_005266524.2:c.617-23_617-22del	XP_005266581.1:n.617-23_617-22del
XM_005266525.2:c.617-23_617-22del	XP_005266582.1:n.617-23_617-22del
XM_006719867.2:c.599-23_599-22del	XP_006719930.1:n.599-23_599-22del
XM_011535229.1:c.617-23_617-22del	XP_011533531.1:n.617-23_617-22del
XM_011535230.1:c.617-23_617-22del	XP_011533532.1:n.617-23_617-22del
XM_011535231.1:c.617-23_617-22del	XP_011533533.1:n.617-23_617-22del
XM_011535232.1:c.455-23_455-22del	XP_011533534.1:n.455-23_455-22del
XM_011535233.1:c.209-23_209-22del	XP_011533535.1:n.209-23_209-22del
XM_006719867.4:c.599-23_599-22del	XP_006719930.1:n.599-23_599-22del
XM_011535230.2:c.617-23_617-22del	XP_011533532.1:n.617-23_617-22del
XM_011535231.2:c.617-23_617-22del	XP_011533533.1:n.617-23_617-22del
XM_011535233.2:c.209-23_209-22del	XP_011533535.1:n.209-23_209-22del
XM_017020747.1:c.617-23_617-22del	XP_016876236.1:n.617-23_617-22del
NM_024570.4:c.617-23_617-22del MANE Select	NP_078846.2:n.617-23_617-22del