Canonical Allele Identifier: CA388259850

Gene: RNASEH2B

Linked Data

• MyVariant Identifiers: chr13:g.51522161T>G (hg19) ; chr13:g.50948025T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.50948025T>G , CM000675.2:g.50948025T>G	GRCh38
NC_000013.10:g.51522161T>G , CM000675.1:g.51522161T>G	GRCh37
NC_000013.9:g.50420162T>G	NCBI36
NG_009055.1:g.43270T>G , LRG_279:g.43270T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336617.8:c.655T>G MANE Select	ENSP00000337623.2:p.Tyr219Asp
ENST00000422660.6:c.655T>G	ENSP00000389877.1:p.Tyr219Asp
ENST00000459681.3:n.338T>G
ENST00000495244.7:n.666T>G
ENST00000611510.5:c.565T>G	ENSP00000481236.3:p.Tyr189Asp
ENST00000616907.2:c.655T>G	ENSP00000482701.2:p.Tyr219Asp
ENST00000642207.1:c.394T>G
ENST00000642454.1:c.565T>G	ENSP00000494221.1:p.Tyr189Asp
ENST00000642721.1:c.655T>G	ENSP00000495650.1:p.Tyr219Asp
ENST00000642995.1:c.538T>G	ENSP00000493499.1:p.Tyr180Asp
ENST00000643159.1:c.565T>G	ENSP00000495587.1:p.Tyr189Asp
ENST00000643215.1:c.525T>G
ENST00000643405.1:c.303T>G
ENST00000643529.1:c.168T>G
ENST00000643682.1:c.655T>G	ENSP00000493655.1:p.Tyr219Asp
ENST00000643774.1:c.619T>G	ENSP00000495482.1:p.Tyr207Asp
ENST00000644034.1:c.103T>G	ENSP00000495456.1:p.Tyr35Asp
ENST00000644183.1:c.545T>G	ENSP00000495657.1:n.545T>G
ENST00000644297.1:c.*513T>G	ENSP00000495519.1:n.*513T>G
ENST00000644420.1:n.681T>G
ENST00000644425.1:c.606T>G
ENST00000644518.1:c.*522T>G	ENSP00000495793.1:n.*522T>G
ENST00000645188.1:c.646T>G	ENSP00000496224.1:p.Tyr216Asp
ENST00000645201.1:n.52T>G
ENST00000645333.1:n.587T>G
ENST00000645370.1:c.490T>G	ENSP00000494019.1:p.Tyr164Asp
ENST00000645618.1:c.565T>G	ENSP00000495429.1:p.Tyr189Asp
ENST00000645712.1:n.679T>G
ENST00000645955.1:c.655T>G	ENSP00000495755.1:p.Tyr219Asp
ENST00000645990.1:c.655T>G	ENSP00000496571.1:p.Tyr219Asp
ENST00000646092.1:c.619T>G	ENSP00000496293.1:p.Tyr207Asp
ENST00000646279.1:n.952T>G
ENST00000646339.1:c.317T>G	ENSP00000495773.1:n.317T>G
ENST00000646709.1:c.565T>G	ENSP00000495278.1:p.Tyr189Asp
ENST00000646731.1:c.646T>G	ENSP00000493828.1:p.Tyr216Asp
ENST00000646960.1:c.655T>G	ENSP00000496481.1:p.Tyr219Asp
ENST00000646964.1:n.1294T>G
ENST00000647387.1:c.565T>G	ENSP00000495487.1:p.Tyr189Asp
ENST00000336617.7:c.655T>G	ENSP00000337623.2:p.Tyr219Asp
ENST00000422660.5:c.655T>G	ENSP00000389877.1:p.Tyr219Asp
ENST00000495244.6:n.666T>G
ENST00000611510.4:c.655T>G	ENSP00000481236.2:p.Tyr219Asp
ENST00000613449.4:n.2717T>G
ENST00000616907.1:c.38T>G
ENST00000621641.1:n.243T>G
NM_001142279.2:c.655T>G , LRG_279t1:c.655T>G	NP_001135751.1:p.Tyr219Asp
NM_024570.3:c.655T>G , LRG_279t2:c.655T>G	NP_078846.2:p.Tyr219Asp
XM_005266524.2:c.655T>G	XP_005266581.1:p.Tyr219Asp
XM_005266525.2:c.655T>G	XP_005266582.1:p.Tyr219Asp
XM_006719867.2:c.637T>G	XP_006719930.1:p.Tyr213Asp
XM_011535229.1:c.655T>G	XP_011533531.1:p.Tyr219Asp
XM_011535230.1:c.655T>G	XP_011533532.1:p.Tyr219Asp
XM_011535231.1:c.655T>G	XP_011533533.1:p.Tyr219Asp
XM_011535232.1:c.493T>G	XP_011533534.1:p.Tyr165Asp
XM_011535233.1:c.247T>G	XP_011533535.1:p.Tyr83Asp
XM_006719867.4:c.637T>G	XP_006719930.1:p.Tyr213Asp
XM_011535230.2:c.655T>G	XP_011533532.1:p.Tyr219Asp
XM_011535231.2:c.655T>G	XP_011533533.1:p.Tyr219Asp
XM_011535233.2:c.247T>G	XP_011533535.1:p.Tyr83Asp
XM_017020747.1:c.655T>G	XP_016876236.1:p.Tyr219Asp
NM_024570.4:c.655T>G MANE Select	NP_078846.2:p.Tyr219Asp