Canonical Allele Identifier: CA1503628430
Gene: LRBA HGNC NCBI

Linked Data

dbSNP Id: rs1749511869

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.150844201_150844211del , CM000666.2:g.150844201_150844211del GRCh38
NC_000004.11:g.151765353_151765363del , CM000666.1:g.151765353_151765363del GRCh37
NC_000004.10:g.151984803_151984813del NCBI36
NG_032855.1:g.176287_176297del

Transcript Alleles

HGVS Amino-acid Change
ENST00000651695.2:c.4462-4_4468del
ENST00000697129.1:n.2789-4_2795del
ENST00000357115.9:c.4462-4_4468del
ENST00000651035.1:c.4462-4_4468del
ENST00000651695.1:c.2176-4_2182del
ENST00000651943.2:c.4462-4_4468del
ENST00000357115.7:c.4462-4_4468del
ENST00000502839.1:c.193-4_199del
ENST00000507224.5:c.4462-4_4468del
ENST00000509835.5:c.420-4_426del
ENST00000510413.5:c.4462-4_4468del
NM_001199282.2:c.4462-4_4468del
NM_006726.4:c.4462-4_4468del
XM_005263372.2:c.4462-4_4468del
XM_005263373.1:c.4462-4_4468del
XM_005263374.2:c.4462-4_4468del
XM_005263375.2:c.4462-4_4468del
XM_005263377.2:c.4462-4_4468del
XM_011532434.1:c.4462-4_4468del
NM_001364905.1:c.4462-4_4468del
XM_005263372.3:c.4462-4_4468del
XM_005263373.3:c.4462-4_4468del
XM_005263374.3:c.4462-4_4468del
XM_011532434.2:c.4462-4_4468del
XM_017008872.2:c.4462-4_4468del
NM_001367550.1:c.4462-4_4468del