Canonical Allele Identifier: CA1866959961
Gene: GABBR2 HGNC NCBI

Linked Data

dbSNP Id: rs1831958243

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98380724del , CM000671.2:g.98380724del GRCh38
NC_000009.11:g.101143006del , CM000671.1:g.101143006del GRCh37
NC_000009.10:g.100182827del NCBI36
NG_016426.1:g.333478del

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.1662+4920del MANE Select ENSP00000259455.2:n.1662+4920del
ENST00000637410.1:n.1440+4920del
ENST00000259455.3:c.1662+4920del ENSP00000259455.2:n.1662+4920del
ENST00000634314.1:n.167+4920del
NM_005458.7:c.1662+4920del NP_005449.5:n.1662+4920del
XM_005252316.3:c.888+4920del XP_005252373.1:n.888+4920del
XM_005252316.5:c.888+4920del XP_005252373.1:n.888+4920del
XM_017015331.2:c.1368+4920del XP_016870820.1:n.1368+4920del
XM_017015332.2:c.888+4920del XP_016870821.1:n.888+4920del
NM_005458.8:c.1662+4920del MANE Select NP_005449.5:n.1662+4920del