Canonical Allele Identifier: CA2144362617

Gene: RAD51B

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.68564496C= , CM000676.2:g.68564496C=	GRCh38
NC_000014.8:g.69031213C= , CM000676.1:g.69031213C=	GRCh37
NC_000014.7:g.68100966C=	NCBI36
NG_023267.1:g.749705C=
NG_023267.2:g.749718C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478014.5:n.383+96246C=
ENST00000487270.5:c.1037-29989C=	ENSP00000419471.1:n.1037-29989C=
ENST00000487861.5:c.1037-46510C=	ENSP00000419881.1:n.1037-46510C=
ENST00000488612.5:c.1037-86285C=	ENSP00000420061.1:n.1037-86285C=
ENST00000553595.5:n.614-118441C=
ENST00000554244.5:n.487+878C=
ENST00000556251.1:n.63+18872C=
NM_133509.3:c.1037-29989C=	NP_598193.2:n.1037-29989C=
XM_005267963.2:c.1036+96246C=	XP_005268020.1:n.1036+96246C=
XM_011537047.1:c.1037-43400C=	XP_011535349.1:n.1037-43400C=
XM_011537048.1:c.1037-46510C=	XP_011535350.1:n.1037-46510C=
XM_011537049.1:c.*942C=	XP_011535351.1:n.*942C=
XR_943503.1:n.1407+96246C=
XR_943975.1:n.87+653G=
NM_001321809.1:c.1037-38167C=	NP_001308738.1:n.1037-38167C=
NM_001321810.1:c.1037-38167C=	NP_001308739.1:n.1037-38167C=
NM_001321815.1:c.923-46662C=	NP_001308744.1:n.923-46662C=
NM_001321818.1:c.1036+96246C=	NP_001308747.1:n.1036+96246C=
NM_001321821.1:c.1037-46510C=	NP_001308750.1:n.1037-46510C=
XM_017021546.1:c.734-46510C=	XP_016877035.1:n.734-46510C=
XM_017021547.1:c.680-46510C=	XP_016877036.1:n.680-46510C=
XM_017021548.1:c.305-46510C=	XP_016877037.1:n.305-46510C=
NM_133509.4:c.1037-29989C=	NP_598193.2:n.1037-29989C=
NM_001321809.2:c.1037-38167C=	NP_001308738.1:n.1037-38167C=
NM_001321810.2:c.1037-38167C=	NP_001308739.1:n.1037-38167C=
NM_001321818.2:c.1036+96246C=	NP_001308747.1:n.1036+96246C=
NM_001321821.2:c.1037-46510C=	NP_001308750.1:n.1037-46510C=
NM_133509.5:c.1037-29989C=	NP_598193.2:n.1037-29989C=