Canonical Allele Identifier: CA2839876656

Gene: RAD51B

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.68564549T>C , CM000676.2:g.68564549T>C	GRCh38
NC_000014.8:g.69031266T>C , CM000676.1:g.69031266T>C	GRCh37
NC_000014.7:g.68101019T>C	NCBI36
NG_023267.1:g.749758T>C
NG_023267.2:g.749771T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478014.5:n.383+96299T>C
ENST00000487270.5:c.1037-29936T>C	ENSP00000419471.1:n.1037-29936T>C
ENST00000487861.5:c.1037-46457T>C	ENSP00000419881.1:n.1037-46457T>C
ENST00000488612.5:c.1037-86232T>C	ENSP00000420061.1:n.1037-86232T>C
ENST00000553595.5:n.614-118388T>C
ENST00000554244.5:n.487+931T>C
ENST00000556251.1:n.63+18925T>C
NM_133509.3:c.1037-29936T>C	NP_598193.2:n.1037-29936T>C
XM_005267963.2:c.1036+96299T>C	XP_005268020.1:n.1036+96299T>C
XM_011537047.1:c.1037-43347T>C	XP_011535349.1:n.1037-43347T>C
XM_011537048.1:c.1037-46457T>C	XP_011535350.1:n.1037-46457T>C
XM_011537049.1:c.*995T>C	XP_011535351.1:n.*995T>C
XR_943503.1:n.1407+96299T>C
XR_943975.1:n.87+600A>G
NM_001321809.1:c.1037-38114T>C	NP_001308738.1:n.1037-38114T>C
NM_001321810.1:c.1037-38114T>C	NP_001308739.1:n.1037-38114T>C
NM_001321815.1:c.923-46609T>C	NP_001308744.1:n.923-46609T>C
NM_001321818.1:c.1036+96299T>C	NP_001308747.1:n.1036+96299T>C
NM_001321821.1:c.1037-46457T>C	NP_001308750.1:n.1037-46457T>C
XM_017021546.1:c.734-46457T>C	XP_016877035.1:n.734-46457T>C
XM_017021547.1:c.680-46457T>C	XP_016877036.1:n.680-46457T>C
XM_017021548.1:c.305-46457T>C	XP_016877037.1:n.305-46457T>C
NM_133509.4:c.1037-29936T>C	NP_598193.2:n.1037-29936T>C
NM_001321809.2:c.1037-38114T>C	NP_001308738.1:n.1037-38114T>C
NM_001321810.2:c.1037-38114T>C	NP_001308739.1:n.1037-38114T>C
NM_001321818.2:c.1036+96299T>C	NP_001308747.1:n.1036+96299T>C
NM_001321821.2:c.1037-46457T>C	NP_001308750.1:n.1037-46457T>C
NM_133509.5:c.1037-29936T>C	NP_598193.2:n.1037-29936T>C