Canonical Allele Identifier: CA2144401705

Gene: RAD51B

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.68653768C= , CM000676.2:g.68653768C=	GRCh38
NC_000014.8:g.69120485C= , CM000676.1:g.69120485C=	GRCh37
NC_000014.7:g.68190238C=	NCBI36
NG_023267.2:g.838990C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001321818.1:c.1037-29169C=	NP_001308747.1:n.1037-29169C=
NM_001321818.2:c.1037-29169C=	NP_001308747.1:n.1037-29169C=
ENST00000478014.5:n.384-29169C=
ENST00000488612.5:c.*11+2912C=	ENSP00000420061.1:n.*11+2912C=
ENST00000553595.5:n.614-29169C=
ENST00000554244.5:n.488-29169C=
XM_005267963.2:c.1037-29169C=	XP_005268020.1:n.1037-29169C=
XM_011537439.1:c.83-1100G=	XP_011535741.1:n.83-1100G=
XM_011537440.1:c.83-1100G=	XP_011535742.1:n.83-1100G=
XR_429374.2:n.1698-1100G=
XR_943503.1:n.1408-28352C=
XR_943970.1:n.1698-1100G=
XR_943972.1:n.1698-1100G=
XR_943974.1:n.84+1093C=