Canonical Allele Identifier: CA707992590

Gene: RAD51B

Linked Data

• dbSNP Id: rs1428840393
• gnomAD v3: 14-68526181-T-A
• gnomAD v4: 14-68526181-T-A
• MyVariant Identifiers: chr14:g.68992898T>A (hg19) ; chr14:g.68526181T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.68526181T>A , CM000676.2:g.68526181T>A	GRCh38
NC_000014.8:g.68992898T>A , CM000676.1:g.68992898T>A	GRCh37
NC_000014.7:g.68062651T>A	NCBI36
NG_023267.1:g.711390T>A
NG_023267.2:g.711403T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000478014.5:n.383+57931T>A
ENST00000487270.5:c.1036+57931T>A	ENSP00000419471.1:n.1036+57931T>A
ENST00000487861.5:c.1036+57931T>A	ENSP00000419881.1:n.1036+57931T>A
ENST00000488612.5:c.1036+57931T>A	ENSP00000420061.1:n.1036+57931T>A
ENST00000497460.5:n.497-14019T>A
ENST00000553595.5:n.613+114654T>A
ENST00000554244.5:n.419-37369T>A
NM_133509.3:c.1036+57931T>A	NP_598193.2:n.1036+57931T>A
XM_005267963.2:c.1036+57931T>A	XP_005268020.1:n.1036+57931T>A
XM_011537047.1:c.1036+57931T>A	XP_011535349.1:n.1036+57931T>A
XM_011537048.1:c.1036+57931T>A	XP_011535350.1:n.1036+57931T>A
XM_011537049.1:c.1037-37369T>A	XP_011535351.1:n.1037-37369T>A
XR_943503.1:n.1407+57931T>A
NM_001321809.1:c.1036+57931T>A	NP_001308738.1:n.1036+57931T>A
NM_001321810.1:c.1036+57931T>A	NP_001308739.1:n.1036+57931T>A
NM_001321812.1:c.1037-14019T>A	NP_001308741.1:n.1037-14019T>A
NM_001321814.1:c.1037-14019T>A	NP_001308743.1:n.1037-14019T>A
NM_001321815.1:c.922+57931T>A	NP_001308744.1:n.922+57931T>A
NM_001321818.1:c.1036+57931T>A	NP_001308747.1:n.1036+57931T>A
NM_001321821.1:c.1036+57931T>A	NP_001308750.1:n.1036+57931T>A
XM_017021546.1:c.733+57931T>A	XP_016877035.1:n.733+57931T>A
XM_017021547.1:c.679+57931T>A	XP_016877036.1:n.679+57931T>A
XM_017021548.1:c.304+57931T>A	XP_016877037.1:n.304+57931T>A
NM_133509.4:c.1036+57931T>A	NP_598193.2:n.1036+57931T>A
NM_001321809.2:c.1036+57931T>A	NP_001308738.1:n.1036+57931T>A
NM_001321810.2:c.1036+57931T>A	NP_001308739.1:n.1036+57931T>A
NM_001321814.2:c.1037-14019T>A	NP_001308743.1:n.1037-14019T>A
NM_001321818.2:c.1036+57931T>A	NP_001308747.1:n.1036+57931T>A
NM_001321821.2:c.1036+57931T>A	NP_001308750.1:n.1036+57931T>A
NM_133509.5:c.1036+57931T>A	NP_598193.2:n.1036+57931T>A