Canonical Allele Identifier: CA1159499

Gene: RHBG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.156381425C>T , CM000663.2:g.156381425C>T	GRCh38
NC_000001.10:g.156351216C>T , CM000663.1:g.156351216C>T	GRCh37
NC_000001.9:g.154617840C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537040.6:c.752C>T MANE Select	ENSP00000441197.2:p.Ala251Val
ENST00000451864.6:c.*692C>T	ENSP00000389836.3:n.*692C>T
ENST00000537040.5:c.752C>T	ENSP00000441197.2:p.Ala251Val
ENST00000612897.4:c.*363C>T	ENSP00000477836.1:n.*363C>T
ENST00000613460.4:c.*581C>T	ENSP00000483178.1:n.*581C>T
ENST00000618120.4:n.885C>T
ENST00000620376.4:c.985C>T
NM_001256395.1:c.545C>T	NP_001243324.1:p.Ala182Val
NM_001256396.1:c.662C>T	NP_001243325.1:p.Ala221Val
NM_020407.4:c.752C>T	NP_065140.3:p.Ala251Val
NR_046115.1:n.950C>T
XM_011509794.1:c.989C>T	XP_011508096.1:p.Ala330Val
XM_011509795.1:c.545C>T	XP_011508097.1:p.Ala182Val
XM_011509796.1:c.545C>T	XP_011508098.1:p.Ala182Val
XM_011509797.1:c.545C>T	XP_011508099.1:p.Ala182Val
XM_011509798.1:c.674C>T	XP_011508100.1:p.Ala225Val
XM_011509799.1:c.578C>T	XP_011508101.1:p.Ala193Val
XM_011509800.1:c.266C>T	XP_011508102.1:p.Ala89Val
XR_921898.1:n.791C>T
XR_921899.1:n.791C>T
XR_921900.1:n.917C>T
NR_146763.1:n.1659C>T
NR_146764.1:n.936C>T
NR_146765.1:n.936C>T
XM_011509799.2:c.578C>T	XP_011508101.1:p.Ala193Val
XM_011509800.2:c.266C>T	XP_011508102.1:p.Ala89Val
XM_017001857.1:c.752C>T	XP_016857346.1:p.Ala251Val
XM_017001858.1:c.752C>T	XP_016857347.1:p.Ala251Val
XM_017001859.1:c.251C>T	XP_016857348.1:p.Ala84Val
XR_001737323.1:n.799C>T
XR_001737324.1:n.799C>T
XR_001737325.1:n.910C>T
XR_001737328.1:n.799C>T
XR_001737329.1:n.799C>T
XR_001737330.1:n.799C>T
XR_001737332.1:n.641-643C>T
NM_001256395.2:c.545C>T	NP_001243324.1:p.Ala182Val
NM_001256396.2:c.662C>T	NP_001243325.1:p.Ala221Val
NM_020407.5:c.752C>T MANE Select	NP_065140.3:p.Ala251Val
NR_046115.2:n.928C>T
NR_146763.2:n.1637C>T
NR_146764.2:n.914C>T
NR_146765.2:n.914C>T