Canonical Allele Identifier: CA388259826

Gene: RNASEH2B

Linked Data

• MyVariant Identifiers: chr13:g.51522149C>A (hg19) ; chr13:g.50948013C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.50948013C>A , CM000675.2:g.50948013C>A	GRCh38
NC_000013.10:g.51522149C>A , CM000675.1:g.51522149C>A	GRCh37
NC_000013.9:g.50420150C>A	NCBI36
NG_009055.1:g.43258C>A , LRG_279:g.43258C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336617.8:c.643C>A MANE Select	ENSP00000337623.2:p.Leu215Met
ENST00000422660.6:c.643C>A	ENSP00000389877.1:p.Leu215Met
ENST00000459681.3:n.326C>A
ENST00000495244.7:n.654C>A
ENST00000611510.5:c.553C>A	ENSP00000481236.3:p.Leu185Met
ENST00000616907.2:c.643C>A	ENSP00000482701.2:p.Leu215Met
ENST00000642207.1:c.382C>A
ENST00000642454.1:c.553C>A	ENSP00000494221.1:p.Leu185Met
ENST00000642721.1:c.643C>A	ENSP00000495650.1:p.Leu215Met
ENST00000642995.1:c.526C>A	ENSP00000493499.1:p.Leu176Met
ENST00000643159.1:c.553C>A	ENSP00000495587.1:p.Leu185Met
ENST00000643215.1:c.513C>A
ENST00000643405.1:c.291C>A
ENST00000643529.1:c.156C>A
ENST00000643682.1:c.643C>A	ENSP00000493655.1:p.Leu215Met
ENST00000643774.1:c.607C>A	ENSP00000495482.1:p.Leu203Met
ENST00000644034.1:c.91C>A	ENSP00000495456.1:p.Leu31Met
ENST00000644183.1:c.533C>A	ENSP00000495657.1:n.533C>A
ENST00000644297.1:c.*501C>A	ENSP00000495519.1:n.*501C>A
ENST00000644420.1:n.669C>A
ENST00000644425.1:c.594C>A
ENST00000644518.1:c.*510C>A	ENSP00000495793.1:n.*510C>A
ENST00000645188.1:c.634C>A	ENSP00000496224.1:p.Leu212Met
ENST00000645201.1:n.40C>A
ENST00000645333.1:n.575C>A
ENST00000645370.1:c.478C>A	ENSP00000494019.1:p.Leu160Met
ENST00000645618.1:c.553C>A	ENSP00000495429.1:p.Leu185Met
ENST00000645712.1:n.667C>A
ENST00000645955.1:c.643C>A	ENSP00000495755.1:p.Leu215Met
ENST00000645990.1:c.643C>A	ENSP00000496571.1:p.Leu215Met
ENST00000646092.1:c.607C>A	ENSP00000496293.1:p.Leu203Met
ENST00000646279.1:n.940C>A
ENST00000646339.1:c.305C>A	ENSP00000495773.1:n.305C>A
ENST00000646709.1:c.553C>A	ENSP00000495278.1:p.Leu185Met
ENST00000646731.1:c.634C>A	ENSP00000493828.1:p.Leu212Met
ENST00000646960.1:c.643C>A	ENSP00000496481.1:p.Leu215Met
ENST00000646964.1:n.1282C>A
ENST00000647387.1:c.553C>A	ENSP00000495487.1:p.Leu185Met
ENST00000336617.7:c.643C>A	ENSP00000337623.2:p.Leu215Met
ENST00000422660.5:c.643C>A	ENSP00000389877.1:p.Leu215Met
ENST00000495244.6:n.654C>A
ENST00000611510.4:c.643C>A	ENSP00000481236.2:p.Leu215Met
ENST00000613449.4:n.2705C>A
ENST00000616907.1:c.26C>A
ENST00000621641.1:n.231C>A
NM_001142279.2:c.643C>A , LRG_279t1:c.643C>A	NP_001135751.1:p.Leu215Met
NM_024570.3:c.643C>A , LRG_279t2:c.643C>A	NP_078846.2:p.Leu215Met
XM_005266524.2:c.643C>A	XP_005266581.1:p.Leu215Met
XM_005266525.2:c.643C>A	XP_005266582.1:p.Leu215Met
XM_006719867.2:c.625C>A	XP_006719930.1:p.Leu209Met
XM_011535229.1:c.643C>A	XP_011533531.1:p.Leu215Met
XM_011535230.1:c.643C>A	XP_011533532.1:p.Leu215Met
XM_011535231.1:c.643C>A	XP_011533533.1:p.Leu215Met
XM_011535232.1:c.481C>A	XP_011533534.1:p.Leu161Met
XM_011535233.1:c.235C>A	XP_011533535.1:p.Leu79Met
XM_006719867.4:c.625C>A	XP_006719930.1:p.Leu209Met
XM_011535230.2:c.643C>A	XP_011533532.1:p.Leu215Met
XM_011535231.2:c.643C>A	XP_011533533.1:p.Leu215Met
XM_011535233.2:c.235C>A	XP_011533535.1:p.Leu79Met
XM_017020747.1:c.643C>A	XP_016876236.1:p.Leu215Met
NM_024570.4:c.643C>A MANE Select	NP_078846.2:p.Leu215Met