Canonical Allele Identifier: CA964282250

Gene: RAD51B

Linked Data

• dbSNP Id: rs2081351138
• gnomAD v3: 14-68283130-T-C
• gnomAD v4: 14-68283130-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.68283130T>C , CM000676.2:g.68283130T>C	GRCh38
NC_000014.8:g.68749847T>C , CM000676.1:g.68749847T>C	GRCh37
NC_000014.7:g.67819600T>C	NCBI36
NG_023267.1:g.468339T>C
NG_023267.2:g.468352T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000460526.6:c.757-8754T>C	ENSP00000518559.1:n.757-8754T>C
ENST00000471583.6:c.757-8754T>C MANE Select	ENSP00000418859.1:n.757-8754T>C
ENST00000460526.5:n.76-8754T>C
ENST00000468382.5:n.550-8754T>C
ENST00000469165.6:n.76-8754T>C
ENST00000471583.5:c.757-8754T>C	ENSP00000418859.1:n.757-8754T>C
ENST00000478014.5:n.104-8754T>C
ENST00000479335.5:c.*528-8754T>C	ENSP00000417408.1:n.*528-8754T>C
ENST00000487270.5:c.757-8754T>C	ENSP00000419471.1:n.757-8754T>C
ENST00000487861.5:c.757-8754T>C	ENSP00000419881.1:n.757-8754T>C
ENST00000488612.5:c.757-8754T>C	ENSP00000420061.1:n.757-8754T>C
ENST00000492236.5:n.287-8754T>C
ENST00000497460.5:n.217-8754T>C
ENST00000553595.5:n.413-8754T>C
ENST00000554244.5:n.139-8754T>C
ENST00000557045.5:n.115-8754T>C
NM_002877.5:c.757-8754T>C	NP_002868.1:n.757-8754T>C
NM_133509.3:c.757-8754T>C	NP_598193.2:n.757-8754T>C
NM_133510.3:c.757-8754T>C	NP_598194.1:n.757-8754T>C
XM_005267963.2:c.757-8754T>C	XP_005268020.1:n.757-8754T>C
XM_011537047.1:c.757-8754T>C	XP_011535349.1:n.757-8754T>C
XM_011537048.1:c.757-8754T>C	XP_011535350.1:n.757-8754T>C
XM_011537049.1:c.757-8754T>C	XP_011535351.1:n.757-8754T>C
XR_943503.1:n.1128-8754T>C
NM_001321809.1:c.757-8754T>C	NP_001308738.1:n.757-8754T>C
NM_001321810.1:c.757-8754T>C	NP_001308739.1:n.757-8754T>C
NM_001321812.1:c.757-8754T>C	NP_001308741.1:n.757-8754T>C
NM_001321814.1:c.757-8754T>C	NP_001308743.1:n.757-8754T>C
NM_001321815.1:c.643-8754T>C	NP_001308744.1:n.643-8754T>C
NM_001321817.1:c.400-8754T>C	NP_001308746.1:n.400-8754T>C
NM_001321818.1:c.757-8754T>C	NP_001308747.1:n.757-8754T>C
NM_001321819.1:c.757-8754T>C	NP_001308748.1:n.757-8754T>C
NM_001321821.1:c.757-8754T>C	NP_001308750.1:n.757-8754T>C
XM_017021545.2:c.1051-8754T>C	XP_016877034.1:n.1051-8754T>C
XM_017021546.1:c.454-8754T>C	XP_016877035.1:n.454-8754T>C
XM_017021547.1:c.400-8754T>C	XP_016877036.1:n.400-8754T>C
XM_017021548.1:c.25-8754T>C	XP_016877037.1:n.25-8754T>C
NM_001321817.2:c.400-8754T>C	NP_001308746.1:n.400-8754T>C
NM_002877.6:c.757-8754T>C	NP_002868.1:n.757-8754T>C
NM_133509.4:c.757-8754T>C	NP_598193.2:n.757-8754T>C
NM_133510.4:c.757-8754T>C MANE Select	NP_598194.1:n.757-8754T>C
NM_001321809.2:c.757-8754T>C	NP_001308738.1:n.757-8754T>C
NM_001321810.2:c.757-8754T>C	NP_001308739.1:n.757-8754T>C
NM_001321814.2:c.757-8754T>C	NP_001308743.1:n.757-8754T>C
NM_001321818.2:c.757-8754T>C	NP_001308747.1:n.757-8754T>C
NM_001321821.2:c.757-8754T>C	NP_001308750.1:n.757-8754T>C
NM_133509.5:c.757-8754T>C	NP_598193.2:n.757-8754T>C