Canonical Allele Identifier: CA390170639

Gene: RAD51B

Linked Data

• ClinVar Variation Id: 1676677
• ClinVar RCV Id: RCV002221990
• dbSNP Id: rs1464701988
• gnomAD v2: 14-68331858-T-C
• gnomAD v4: 14-67865141-T-C
• MyVariant Identifiers: chr14:g.68331858T>C (hg19) ; chr14:g.67865141T>C (hg38)
• MutSpliceDB: CA390170639

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67865141T>C , CM000676.2:g.67865141T>C	GRCh38
NC_000014.8:g.68331858T>C , CM000676.1:g.68331858T>C	GRCh37
NC_000014.7:g.67401611T>C	NCBI36
NG_023267.1:g.50350T>C
NG_023267.2:g.50363T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460526.6:c.452+2T>C	ENSP00000518559.1:n.452+2T>C
ENST00000711050.1:n.496+2T>C
ENST00000471583.6:c.452+2T>C MANE Select	ENSP00000418859.1:n.452+2T>C
ENST00000390683.7:c.452+2T>C	ENSP00000375101.4:n.452+2T>C
ENST00000471583.5:c.452+2T>C	ENSP00000418859.1:n.452+2T>C
ENST00000479335.5:c.*223+2T>C	ENSP00000417408.1:n.*223+2T>C
ENST00000487270.5:c.452+2T>C	ENSP00000419471.1:n.452+2T>C
ENST00000487861.5:c.452+2T>C	ENSP00000419881.1:n.452+2T>C
ENST00000488612.5:c.452+2T>C	ENSP00000420061.1:n.452+2T>C
ENST00000553595.5:n.108+2T>C
ENST00000553734.5:n.205+2T>C
ENST00000555907.5:n.303+2T>C
NM_002877.5:c.452+2T>C	NP_002868.1:n.452+2T>C
NM_133509.3:c.452+2T>C	NP_598193.2:n.452+2T>C
NM_133510.3:c.452+2T>C	NP_598194.1:n.452+2T>C
XM_005267963.2:c.452+2T>C	XP_005268020.1:n.452+2T>C
XM_011537047.1:c.452+2T>C	XP_011535349.1:n.452+2T>C
XM_011537048.1:c.452+2T>C	XP_011535350.1:n.452+2T>C
XM_011537049.1:c.452+2T>C	XP_011535351.1:n.452+2T>C
XM_011537050.1:c.452+2T>C	XP_011535352.1:n.452+2T>C
XM_011537051.1:c.452+2T>C	XP_011535353.1:n.452+2T>C
XR_943503.1:n.529+2T>C
NM_001321809.1:c.452+2T>C	NP_001308738.1:n.452+2T>C
NM_001321810.1:c.452+2T>C	NP_001308739.1:n.452+2T>C
NM_001321812.1:c.452+2T>C	NP_001308741.1:n.452+2T>C
NM_001321814.1:c.452+2T>C	NP_001308743.1:n.452+2T>C
NM_001321815.1:c.338+2T>C	NP_001308744.1:n.338+2T>C
NM_001321817.1:c.95+2T>C	NP_001308746.1:n.95+2T>C
NM_001321818.1:c.452+2T>C	NP_001308747.1:n.452+2T>C
NM_001321819.1:c.452+2T>C	NP_001308748.1:n.452+2T>C
NM_001321821.1:c.452+2T>C	NP_001308750.1:n.452+2T>C
XM_011537050.3:c.452+2T>C	XP_011535352.1:n.452+2T>C
XM_017021545.2:c.452+2T>C	XP_016877034.1:n.452+2T>C
XM_017021547.1:c.95+2T>C	XP_016877036.1:n.95+2T>C
NM_001321817.2:c.95+2T>C	NP_001308746.1:n.95+2T>C
NM_002877.6:c.452+2T>C	NP_002868.1:n.452+2T>C
NM_133509.4:c.452+2T>C	NP_598193.2:n.452+2T>C
NM_133510.4:c.452+2T>C MANE Select	NP_598194.1:n.452+2T>C
NM_001321809.2:c.452+2T>C	NP_001308738.1:n.452+2T>C
NM_001321810.2:c.452+2T>C	NP_001308739.1:n.452+2T>C
NM_001321814.2:c.452+2T>C	NP_001308743.1:n.452+2T>C
NM_001321818.2:c.452+2T>C	NP_001308747.1:n.452+2T>C
NM_001321821.2:c.452+2T>C	NP_001308750.1:n.452+2T>C
NM_133509.5:c.452+2T>C	NP_598193.2:n.452+2T>C