Canonical Allele Identifier: CA707992576

Gene: RAD51B

Linked Data

• dbSNP Id: rs1421611359
• MyVariant Identifiers: chr14:g.68992880_68992882del (hg19) ; chr14:g.68526163_68526165del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.68526172_68526174del , CM000676.2:g.68526172_68526174del	GRCh38
NC_000014.8:g.68992889_68992891del , CM000676.1:g.68992889_68992891del	GRCh37
NC_000014.7:g.68062642_68062644del	NCBI36
NG_023267.1:g.711381_711383del
NG_023267.2:g.711394_711396del

Transcript Alleles

HGVS	Amino-acid change
ENST00000478014.5:n.383+57922_383+57924del
ENST00000487270.5:c.1036+57922_1036+57924del	ENSP00000419471.1:n.1036+57922_1036+57924...
ENST00000487861.5:c.1036+57922_1036+57924del	ENSP00000419881.1:n.1036+57922_1036+57924...
ENST00000488612.5:c.1036+57922_1036+57924del	ENSP00000420061.1:n.1036+57922_1036+57924...
ENST00000497460.5:n.497-14028_497-14026del
ENST00000553595.5:n.613+114645_613+114647del
ENST00000554244.5:n.419-37378_419-37376del
NM_133509.3:c.1036+57922_1036+57924del	NP_598193.2:n.1036+57922_1036+57924del
XM_005267963.2:c.1036+57922_1036+57924del	XP_005268020.1:n.1036+57922_1036+57924del...
XM_011537047.1:c.1036+57922_1036+57924del	XP_011535349.1:n.1036+57922_1036+57924del...
XM_011537048.1:c.1036+57922_1036+57924del	XP_011535350.1:n.1036+57922_1036+57924del...
XM_011537049.1:c.1037-37378_1037-37376del	XP_011535351.1:n.1037-37378_1037-37376del...
XR_943503.1:n.1407+57922_1407+57924del
NM_001321809.1:c.1036+57922_1036+57924del	NP_001308738.1:n.1036+57922_1036+57924del...
NM_001321810.1:c.1036+57922_1036+57924del	NP_001308739.1:n.1036+57922_1036+57924del...
NM_001321812.1:c.1037-14028_1037-14026del	NP_001308741.1:n.1037-14028_1037-14026del...
NM_001321814.1:c.1037-14028_1037-14026del	NP_001308743.1:n.1037-14028_1037-14026del...
NM_001321815.1:c.922+57922_922+57924del	NP_001308744.1:n.922+57922_922+57924del
NM_001321818.1:c.1036+57922_1036+57924del	NP_001308747.1:n.1036+57922_1036+57924del...
NM_001321821.1:c.1036+57922_1036+57924del	NP_001308750.1:n.1036+57922_1036+57924del...
XM_017021546.1:c.733+57922_733+57924del	XP_016877035.1:n.733+57922_733+57924del
XM_017021547.1:c.679+57922_679+57924del	XP_016877036.1:n.679+57922_679+57924del
XM_017021548.1:c.304+57922_304+57924del	XP_016877037.1:n.304+57922_304+57924del
NM_133509.4:c.1036+57922_1036+57924del	NP_598193.2:n.1036+57922_1036+57924del
NM_001321809.2:c.1036+57922_1036+57924del	NP_001308738.1:n.1036+57922_1036+57924del...
NM_001321810.2:c.1036+57922_1036+57924del	NP_001308739.1:n.1036+57922_1036+57924del...
NM_001321814.2:c.1037-14028_1037-14026del	NP_001308743.1:n.1037-14028_1037-14026del...
NM_001321818.2:c.1036+57922_1036+57924del	NP_001308747.1:n.1036+57922_1036+57924del...
NM_001321821.2:c.1036+57922_1036+57924del	NP_001308750.1:n.1036+57922_1036+57924del...
NM_133509.5:c.1036+57922_1036+57924del	NP_598193.2:n.1036+57922_1036+57924del