Canonical Allele Identifier: CA1867008298
Gene: GABBR2 HGNC NCBI

Linked Data

dbSNP Id: rs1693677074

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98515489_98515490del , CM000671.2:g.98515489_98515490del GRCh38
NC_000009.11:g.101277771_101277772del , CM000671.1:g.101277771_101277772del GRCh37
NC_000009.10:g.100317592_100317593del NCBI36
NG_016426.1:g.198709_198710del

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.631-18975_631-18974del MANE Select ENSP00000259455.2:n.631-18975_631-18974del
ENST00000637410.1:n.409-18975_409-18974del
ENST00000259455.3:c.631-18975_631-18974del ENSP00000259455.2:n.631-18975_631-18974del
ENST00000477471.1:n.418-18975_418-18974del
ENST00000634227.1:n.405-18975_405-18974del
ENST00000634919.1:n.306+505_306+506del
NM_005458.7:c.631-18975_631-18974del NP_005449.5:n.631-18975_631-18974del
XM_005252316.3:c.-144-18975_-144-18974del XP_005252373.1:n.-144-18975_-144-18974del
XM_005252316.5:c.-144-18975_-144-18974del XP_005252373.1:n.-144-18975_-144-18974del
XM_017015331.2:c.337-18975_337-18974del XP_016870820.1:n.337-18975_337-18974del
NM_005458.8:c.631-18975_631-18974del MANE Select NP_005449.5:n.631-18975_631-18974del