Canonical Allele Identifier: CA2017463097
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13615332_13615333delinsAT , CM000674.2:g.13615332_13615333delinsAT GRCh38
NC_000012.11:g.13768266_13768267delinsAT , CM000674.1:g.13768266_13768267delinsAT GRCh37
NC_000012.10:g.13659533_13659534delinsAT NCBI36
NG_031854.1:g.369756_369757delinsAT
NG_031854.2:g.371680_371681delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.1501-66_1501-65delinsAT MANE Select ENSP00000477455.1:n.1501-66_1501-65delinsAT
ENST00000609686.3:c.1501-66_1501-65delinsAT ENSP00000477455.1:n.1501-66_1501-65delinsAT
NM_000834.3:c.1501-66_1501-65delinsAT NP_000825.2:n.1501-66_1501-65delinsAT
XM_011520628.1:c.1501-66_1501-65delinsAT XP_011518930.1:n.1501-66_1501-65delinsAT
XM_011520629.1:c.1501-66_1501-65delinsAT XP_011518931.1:n.1501-66_1501-65delinsAT
XM_011520630.1:c.1501-66_1501-65delinsAT XP_011518932.1:n.1501-66_1501-65delinsAT
XR_931372.1:n.307+106_307+107delinsAT
XR_931373.1:n.447+106_447+107delinsAT
XR_931374.1:n.246+106_246+107delinsAT
NM_000834.4:c.1501-66_1501-65delinsAT NP_000825.2:n.1501-66_1501-65delinsAT
XM_011520628.2:c.1501-66_1501-65delinsAT XP_011518930.1:n.1501-66_1501-65delinsAT
XM_011520629.2:c.1501-66_1501-65delinsAT XP_011518931.1:n.1501-66_1501-65delinsAT
XM_017019219.2:c.1501-66_1501-65delinsAT XP_016874708.1:n.1501-66_1501-65delinsAT
XR_001749013.1:n.728+106_728+107delinsAT
XR_931372.2:n.444+106_444+107delinsAT
XR_931373.2:n.586+106_586+107delinsAT
NM_000834.5:c.1501-66_1501-65delinsAT MANE Select NP_000825.2:n.1501-66_1501-65delinsAT