Canonical Allele Identifier: CA2144362704
Gene: RAD51B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68564712C= , CM000676.2:g.68564712C= GRCh38
NC_000014.8:g.69031429C= , CM000676.1:g.69031429C= GRCh37
NC_000014.7:g.68101182C= NCBI36
NG_023267.1:g.749921C=
NG_023267.2:g.749934C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000478014.5:n.383+96462C=
ENST00000487270.5:c.1037-29773C= ENSP00000419471.1:n.1037-29773C=
ENST00000487861.5:c.1037-46294C= ENSP00000419881.1:n.1037-46294C=
ENST00000488612.5:c.1037-86069C= ENSP00000420061.1:n.1037-86069C=
ENST00000553595.5:n.614-118225C=
ENST00000554244.5:n.487+1094C=
ENST00000556251.1:n.63+19088C=
NM_133509.3:c.1037-29773C= NP_598193.2:n.1037-29773C=
XM_005267963.2:c.1036+96462C= XP_005268020.1:n.1036+96462C=
XM_011537047.1:c.1037-43184C= XP_011535349.1:n.1037-43184C=
XM_011537048.1:c.1037-46294C= XP_011535350.1:n.1037-46294C=
XM_011537049.1:c.*1158C= XP_011535351.1:n.*1158C=
XR_943503.1:n.1407+96462C=
XR_943975.1:n.87+437G=
NM_001321809.1:c.1037-37951C= NP_001308738.1:n.1037-37951C=
NM_001321810.1:c.1037-37951C= NP_001308739.1:n.1037-37951C=
NM_001321815.1:c.923-46446C= NP_001308744.1:n.923-46446C=
NM_001321818.1:c.1036+96462C= NP_001308747.1:n.1036+96462C=
NM_001321821.1:c.1037-46294C= NP_001308750.1:n.1037-46294C=
XM_017021546.1:c.734-46294C= XP_016877035.1:n.734-46294C=
XM_017021547.1:c.680-46294C= XP_016877036.1:n.680-46294C=
XM_017021548.1:c.305-46294C= XP_016877037.1:n.305-46294C=
NM_133509.4:c.1037-29773C= NP_598193.2:n.1037-29773C=
NM_001321809.2:c.1037-37951C= NP_001308738.1:n.1037-37951C=
NM_001321810.2:c.1037-37951C= NP_001308739.1:n.1037-37951C=
NM_001321818.2:c.1036+96462C= NP_001308747.1:n.1036+96462C=
NM_001321821.2:c.1037-46294C= NP_001308750.1:n.1037-46294C=
NM_133509.5:c.1037-29773C= NP_598193.2:n.1037-29773C=