Canonical Allele Identifier: CA342843951

Gene: RHBG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156378087C>A , CM000663.2:g.156378087C>A	GRCh38
NC_000001.10:g.156347878C>A , CM000663.1:g.156347878C>A	GRCh37
NC_000001.9:g.154614502C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537040.6:c.472C>A MANE Select	ENSP00000441197.2:p.Leu158Met
ENST00000451864.6:c.*301C>A	ENSP00000389836.3:n.*301C>A
ENST00000537040.5:c.472C>A	ENSP00000441197.2:p.Leu158Met
ENST00000612897.4:c.*83C>A	ENSP00000477836.1:n.*83C>A
ENST00000613460.4:c.*301C>A	ENSP00000483178.1:n.*301C>A
ENST00000618120.4:n.605C>A
ENST00000620376.4:c.594C>A
NM_001256395.1:c.265C>A	NP_001243324.1:p.Leu89Met
NM_001256396.1:c.382C>A	NP_001243325.1:p.Leu128Met
NM_020407.4:c.472C>A	NP_065140.3:p.Leu158Met
NR_046115.1:n.656C>A
XM_011509794.1:c.709C>A	XP_011508096.1:p.Leu237Met
XM_011509795.1:c.265C>A	XP_011508097.1:p.Leu89Met
XM_011509796.1:c.265C>A	XP_011508098.1:p.Leu89Met
XM_011509797.1:c.265C>A	XP_011508099.1:p.Leu89Met
XM_011509798.1:c.448-165C>A	XP_011508100.1:n.448-165C>A
XM_011509799.1:c.352-165C>A	XP_011508101.1:n.352-165C>A
XM_011509800.1:c.188-3260C>A	XP_011508102.1:n.188-3260C>A
XR_921898.1:n.511C>A
XR_921899.1:n.511C>A
XR_921900.1:n.526C>A
NR_146763.1:n.1379C>A
NR_146764.1:n.656C>A
NR_146765.1:n.656C>A
XM_011509799.2:c.352-165C>A	XP_011508101.1:n.352-165C>A
XM_011509800.2:c.188-3260C>A	XP_011508102.1:n.188-3260C>A
XM_017001857.1:c.472C>A	XP_016857346.1:p.Leu158Met
XM_017001858.1:c.472C>A	XP_016857347.1:p.Leu158Met
XM_017001859.1:c.25-165C>A	XP_016857348.1:n.25-165C>A
XR_001737323.1:n.519C>A
XR_001737324.1:n.519C>A
XR_001737325.1:n.519C>A
XR_001737328.1:n.519C>A
XR_001737329.1:n.519C>A
XR_001737330.1:n.519C>A
XR_001737332.1:n.519C>A
NM_001256395.2:c.265C>A	NP_001243324.1:p.Leu89Met
NM_001256396.2:c.382C>A	NP_001243325.1:p.Leu128Met
NM_020407.5:c.472C>A MANE Select	NP_065140.3:p.Leu158Met
NR_046115.2:n.634C>A
NR_146763.2:n.1357C>A
NR_146764.2:n.634C>A
NR_146765.2:n.634C>A