Canonical Allele Identifier: CA2144362625

Gene: RAD51B

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.68564510C= , CM000676.2:g.68564510C=	GRCh38
NC_000014.8:g.69031227C= , CM000676.1:g.69031227C=	GRCh37
NC_000014.7:g.68100980C=	NCBI36
NG_023267.1:g.749719C=
NG_023267.2:g.749732C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000478014.5:n.383+96260C=
ENST00000487270.5:c.1037-29975C=	ENSP00000419471.1:n.1037-29975C=
ENST00000487861.5:c.1037-46496C=	ENSP00000419881.1:n.1037-46496C=
ENST00000488612.5:c.1037-86271C=	ENSP00000420061.1:n.1037-86271C=
ENST00000553595.5:n.614-118427C=
ENST00000554244.5:n.487+892C=
ENST00000556251.1:n.63+18886C=
NM_133509.3:c.1037-29975C=	NP_598193.2:n.1037-29975C=
XM_005267963.2:c.1036+96260C=	XP_005268020.1:n.1036+96260C=
XM_011537047.1:c.1037-43386C=	XP_011535349.1:n.1037-43386C=
XM_011537048.1:c.1037-46496C=	XP_011535350.1:n.1037-46496C=
XM_011537049.1:c.*956C=	XP_011535351.1:n.*956C=
XR_943503.1:n.1407+96260C=
XR_943975.1:n.87+639G=
NM_001321809.1:c.1037-38153C=	NP_001308738.1:n.1037-38153C=
NM_001321810.1:c.1037-38153C=	NP_001308739.1:n.1037-38153C=
NM_001321815.1:c.923-46648C=	NP_001308744.1:n.923-46648C=
NM_001321818.1:c.1036+96260C=	NP_001308747.1:n.1036+96260C=
NM_001321821.1:c.1037-46496C=	NP_001308750.1:n.1037-46496C=
XM_017021546.1:c.734-46496C=	XP_016877035.1:n.734-46496C=
XM_017021547.1:c.680-46496C=	XP_016877036.1:n.680-46496C=
XM_017021548.1:c.305-46496C=	XP_016877037.1:n.305-46496C=
NM_133509.4:c.1037-29975C=	NP_598193.2:n.1037-29975C=
NM_001321809.2:c.1037-38153C=	NP_001308738.1:n.1037-38153C=
NM_001321810.2:c.1037-38153C=	NP_001308739.1:n.1037-38153C=
NM_001321818.2:c.1036+96260C=	NP_001308747.1:n.1036+96260C=
NM_001321821.2:c.1037-46496C=	NP_001308750.1:n.1037-46496C=
NM_133509.5:c.1037-29975C=	NP_598193.2:n.1037-29975C=