Canonical Allele Identifier: CA2017450535
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13611609_13611610delinsGT , CM000674.2:g.13611609_13611610delinsGT GRCh38
NC_000012.11:g.13764543_13764544delinsGT , CM000674.1:g.13764543_13764544delinsGT GRCh37
NC_000012.10:g.13655810_13655811delinsGT NCBI36
NG_031854.1:g.373479_373480delinsAC
NG_031854.2:g.375403_375404delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.1780+115_1780+116delinsAC MANE Select ENSP00000477455.1:n.1780+115_1780+116delinsAC
ENST00000609686.3:c.1780+115_1780+116delinsAC ENSP00000477455.1:n.1780+115_1780+116delinsAC
NM_000834.3:c.1780+115_1780+116delinsAC NP_000825.2:n.1780+115_1780+116delinsAC
XM_011520628.1:c.1780+115_1780+116delinsAC XP_011518930.1:n.1780+115_1780+116delinsAC
XM_011520629.1:c.1780+115_1780+116delinsAC XP_011518931.1:n.1780+115_1780+116delinsAC
XM_011520630.1:c.1780+115_1780+116delinsAC XP_011518932.1:n.1780+115_1780+116delinsAC
XR_931372.1:n.179-3489_179-3488delinsGT
XR_931373.1:n.318+2852_318+2853delinsGT
XR_931374.1:n.117+1009_117+1010delinsGT
NM_000834.4:c.1780+115_1780+116delinsAC NP_000825.2:n.1780+115_1780+116delinsAC
XM_011520628.2:c.1780+115_1780+116delinsAC XP_011518930.1:n.1780+115_1780+116delinsAC
XM_011520629.2:c.1780+115_1780+116delinsAC XP_011518931.1:n.1780+115_1780+116delinsAC
XM_017019219.2:c.1780+115_1780+116delinsAC XP_016874708.1:n.1780+115_1780+116delinsAC
XR_001749013.1:n.599+1009_599+1010delinsGT
XR_931372.2:n.316-3489_316-3488delinsGT
XR_931373.2:n.457+2852_457+2853delinsGT
NM_000834.5:c.1780+115_1780+116delinsAC MANE Select NP_000825.2:n.1780+115_1780+116delinsAC