Canonical Allele Identifier: CA2017614079
Gene: GRIN2B HGNC NCBI

Linked Data

dbSNP Id: rs1867333606

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13944823_13944824dup , CM000674.2:g.13944823_13944824dup GRCh38
NC_000012.11:g.14097757_14097758dup , CM000674.1:g.14097757_14097758dup GRCh37
NC_000012.10:g.13989024_13989025dup NCBI36
NG_031854.1:g.40268_40269dup
NG_031854.2:g.42192_42193dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.-19+35107_-19+35108dup MANE Select ENSP00000477455.1:n.-19+35107_-19+35108dup
ENST00000630791.2:c.-19+35107_-19+35108dup ENSP00000486677.2:n.-19+35107_-19+35108dup
ENST00000609686.3:c.-19+35107_-19+35108dup ENSP00000477455.1:n.-19+35107_-19+35108dup
ENST00000627535.2:c.-19+35107_-19+35108dup ENSP00000486411.1:n.-19+35107_-19+35108dup
ENST00000630791.1:c.-19+35107_-19+35108dup ENSP00000486677.1:n.-19+35107_-19+35108dup
NM_000834.3:c.-19+35107_-19+35108dup NP_000825.2:n.-19+35107_-19+35108dup
XM_011520628.1:c.-19+35107_-19+35108dup XP_011518930.1:n.-19+35107_-19+35108dup
XM_011520629.1:c.-19+35107_-19+35108dup XP_011518931.1:n.-19+35107_-19+35108dup
XM_011520630.1:c.-19+35107_-19+35108dup XP_011518932.1:n.-19+35107_-19+35108dup
NM_000834.4:c.-19+35107_-19+35108dup NP_000825.2:n.-19+35107_-19+35108dup
XM_011520628.2:c.-19+35107_-19+35108dup XP_011518930.1:n.-19+35107_-19+35108dup
XM_011520629.2:c.-19+35107_-19+35108dup XP_011518931.1:n.-19+35107_-19+35108dup
XM_017019219.2:c.-19+35107_-19+35108dup XP_016874708.1:n.-19+35107_-19+35108dup
NM_000834.5:c.-19+35107_-19+35108dup MANE Select NP_000825.2:n.-19+35107_-19+35108dup