Canonical Allele Identifier: CA2091107300

Gene: RNASEH2B

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.50943304_50943305delinsCT , CM000675.2:g.50943304_50943305delinsCT	GRCh38
NC_000013.10:g.51517440_51517441delinsCT , CM000675.1:g.51517440_51517441delinsCT	GRCh37
NC_000013.9:g.50415441_50415442delinsCT	NCBI36
NG_009055.1:g.38549_38550delinsCT , LRG_279:g.38549_38550delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336617.8:c.437-17_437-16delinsCT MANE Select	ENSP00000337623.2:n.437-17_437-16delinsCT
ENST00000422660.6:c.437-17_437-16delinsCT	ENSP00000389877.1:n.437-17_437-16delinsCT
ENST00000459681.3:n.120-17_120-16delinsCT
ENST00000495244.7:n.448-17_448-16delinsCT
ENST00000611510.5:c.347-17_347-16delinsCT	ENSP00000481236.3:n.347-17_347-16delinsCT
ENST00000616907.2:c.437-17_437-16delinsCT	ENSP00000482701.2:n.437-17_437-16delinsCT
ENST00000642207.1:c.176-17_176-16delinsCT
ENST00000642454.1:c.347-17_347-16delinsCT	ENSP00000494221.1:n.347-17_347-16delinsCT
ENST00000642721.1:c.437-17_437-16delinsCT	ENSP00000495650.1:n.437-17_437-16delinsCT
ENST00000642995.1:c.329-26_329-25delinsCT	ENSP00000493499.1:n.329-26_329-25delinsCT
ENST00000643159.1:c.347-17_347-16delinsCT	ENSP00000495587.1:n.347-17_347-16delinsCT
ENST00000643215.1:c.307-17_307-16delinsCT
ENST00000643405.1:c.85-17_85-16delinsCT
ENST00000643462.1:c.*252-17_*252-16delinsCT	ENSP00000496130.1:n.*252-17_*252-16delinsCT
ENST00000643682.1:c.437-17_437-16delinsCT	ENSP00000493655.1:n.437-17_437-16delinsCT
ENST00000643774.1:c.401-17_401-16delinsCT	ENSP00000495482.1:n.401-17_401-16delinsCT
ENST00000644034.1:c.65-4683_65-4682delinsCT	ENSP00000495456.1:n.65-4683_65-4682delinsCT
ENST00000644183.1:c.327-17_327-16delinsCT	ENSP00000495657.1:n.327-17_327-16delinsCT
ENST00000644297.1:c.*304-26_*304-25delinsCT	ENSP00000495519.1:n.*304-26_*304-25delinsCT
ENST00000644420.1:n.463-17_463-16delinsCT
ENST00000644425.1:c.388-17_388-16delinsCT
ENST00000644518.1:c.*304-17_*304-16delinsCT	ENSP00000495793.1:n.*304-17_*304-16delinsCT
ENST00000645188.1:c.437-26_437-25delinsCT	ENSP00000496224.1:n.437-26_437-25delinsCT
ENST00000645333.1:n.369-17_369-16delinsCT
ENST00000645370.1:c.272-17_272-16delinsCT	ENSP00000494019.1:n.272-17_272-16delinsCT
ENST00000645618.1:c.347-17_347-16delinsCT	ENSP00000495429.1:n.347-17_347-16delinsCT
ENST00000645712.1:n.470-26_470-25delinsCT
ENST00000645955.1:c.437-17_437-16delinsCT	ENSP00000495755.1:n.437-17_437-16delinsCT
ENST00000645990.1:c.437-17_437-16delinsCT	ENSP00000496571.1:n.437-17_437-16delinsCT
ENST00000646092.1:c.401-17_401-16delinsCT	ENSP00000496293.1:n.401-17_401-16delinsCT
ENST00000646279.1:n.734-17_734-16delinsCT
ENST00000646339.1:c.99-17_99-16delinsCT	ENSP00000495773.1:n.99-17_99-16delinsCT
ENST00000646709.1:c.347-17_347-16delinsCT	ENSP00000495278.1:n.347-17_347-16delinsCT
ENST00000646731.1:c.437-26_437-25delinsCT	ENSP00000493828.1:n.437-26_437-25delinsCT
ENST00000646960.1:c.437-17_437-16delinsCT	ENSP00000496481.1:n.437-17_437-16delinsCT
ENST00000646964.1:n.1076-17_1076-16delinsCT
ENST00000647387.1:c.347-17_347-16delinsCT	ENSP00000495487.1:n.347-17_347-16delinsCT
ENST00000336617.7:c.437-17_437-16delinsCT	ENSP00000337623.2:n.437-17_437-16delinsCT
ENST00000422660.5:c.437-17_437-16delinsCT	ENSP00000389877.1:n.437-17_437-16delinsCT
ENST00000495244.6:n.448-17_448-16delinsCT
ENST00000611510.4:c.437-17_437-16delinsCT	ENSP00000481236.2:n.437-17_437-16delinsCT
ENST00000613449.4:n.2482_2483delinsCT
ENST00000621641.1:n.8_9delinsCT
NM_001142279.2:c.437-17_437-16delinsCT , LRG_279t1:c.437-17_437-16delinsCT	NP_001135751.1:n.437-17_437-16delinsCT
NM_024570.3:c.437-17_437-16delinsCT , LRG_279t2:c.437-17_437-16delinsCT	NP_078846.2:n.437-17_437-16delinsCT
XM_005266524.2:c.437-17_437-16delinsCT	XP_005266581.1:n.437-17_437-16delinsCT
XM_005266525.2:c.437-17_437-16delinsCT	XP_005266582.1:n.437-17_437-16delinsCT
XM_006719867.2:c.419-17_419-16delinsCT	XP_006719930.1:n.419-17_419-16delinsCT
XM_011535229.1:c.437-17_437-16delinsCT	XP_011533531.1:n.437-17_437-16delinsCT
XM_011535230.1:c.437-17_437-16delinsCT	XP_011533532.1:n.437-17_437-16delinsCT
XM_011535231.1:c.437-17_437-16delinsCT	XP_011533533.1:n.437-17_437-16delinsCT
XM_011535232.1:c.275-17_275-16delinsCT	XP_011533534.1:n.275-17_275-16delinsCT
XM_011535233.1:c.29-17_29-16delinsCT	XP_011533535.1:n.29-17_29-16delinsCT
XM_011535234.1:c.437-17_437-16delinsCT	XP_011533536.1:n.437-17_437-16delinsCT
XM_006719867.4:c.419-17_419-16delinsCT	XP_006719930.1:n.419-17_419-16delinsCT
XM_011535230.2:c.437-17_437-16delinsCT	XP_011533532.1:n.437-17_437-16delinsCT
XM_011535231.2:c.437-17_437-16delinsCT	XP_011533533.1:n.437-17_437-16delinsCT
XM_011535233.2:c.29-17_29-16delinsCT	XP_011533535.1:n.29-17_29-16delinsCT
XM_017020747.1:c.437-17_437-16delinsCT	XP_016876236.1:n.437-17_437-16delinsCT
NM_024570.4:c.437-17_437-16delinsCT MANE Select	NP_078846.2:n.437-17_437-16delinsCT