Canonical Allele Identifier: CA1159707

Gene: RHBG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156384538A>G , CM000663.2:g.156384538A>G	GRCh38
NC_000001.10:g.156354329A>G , CM000663.1:g.156354329A>G	GRCh37
NC_000001.9:g.154620953A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537040.6:c.1246A>G MANE Select	ENSP00000441197.2:p.Lys416Glu
ENST00000451864.6:c.*1161A>G	ENSP00000389836.3:n.*1161A>G
ENST00000494874.1:n.182-28A>G
ENST00000537040.5:c.1246A>G	ENSP00000441197.2:p.Lys416Glu
ENST00000612897.4:c.*857A>G	ENSP00000477836.1:n.*857A>G
ENST00000613460.4:c.*1075A>G	ENSP00000483178.1:n.*1075A>G
ENST00000618120.4:n.1925A>G
ENST00000620376.4:c.1479A>G
ENST00000622297.1:n.655A>G
NM_001256395.1:c.1039A>G	NP_001243324.1:p.Lys347Glu
NM_001256396.1:c.1156A>G	NP_001243325.1:p.Lys386Glu
NM_020407.4:c.1246A>G	NP_065140.3:p.Lys416Glu
NR_046115.1:n.1444A>G
XM_011509794.1:c.1483A>G	XP_011508096.1:p.Lys495Glu
XM_011509795.1:c.1039A>G	XP_011508097.1:p.Lys347Glu
XM_011509798.1:c.1168A>G	XP_011508100.1:p.Lys390Glu
XM_011509799.1:c.1072A>G	XP_011508101.1:p.Lys358Glu
XM_011509800.1:c.760A>G	XP_011508102.1:p.Lys254Glu
XR_921898.1:n.1398A>G
XR_921899.1:n.1371A>G
XR_921900.1:n.1386A>G
NR_146763.1:n.2266A>G
NR_146764.1:n.1543A>G
NR_146765.1:n.1646A>G
XM_011509799.2:c.1072A>G	XP_011508101.1:p.Lys358Glu
XM_011509800.2:c.760A>G	XP_011508102.1:p.Lys254Glu
XM_017001859.1:c.745A>G	XP_016857348.1:p.Lys249Glu
XR_001737323.1:n.1406A>G
XR_001737324.1:n.1379A>G
XR_001737325.1:n.1379A>G
XR_001737328.1:n.1952A>G
XR_001737329.1:n.1925A>G
XR_001737332.1:n.1454A>G
NM_001256395.2:c.1039A>G	NP_001243324.1:p.Lys347Glu
NM_001256396.2:c.1156A>G	NP_001243325.1:p.Lys386Glu
NM_020407.5:c.1246A>G MANE Select	NP_065140.3:p.Lys416Glu
NR_046115.2:n.1422A>G
NR_146763.2:n.2244A>G
NR_146764.2:n.1521A>G
NR_146765.2:n.1624A>G