Canonical Allele Identifier: CA6461175
Gene: GRIN2B HGNC NCBI

Linked Data

dbSNP Id: rs746849499

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13611691dup , CM000674.2:g.13611691dup GRCh38
NC_000012.11:g.13764625dup , CM000674.1:g.13764625dup GRCh37
NC_000012.10:g.13655892dup NCBI36
NG_031854.1:g.373404dup
NG_031854.2:g.375328dup

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.1780+40dup MANE Select ENSP00000477455.1:n.1780+40dup
ENST00000609686.3:c.1780+40dup ENSP00000477455.1:n.1780+40dup
NM_000834.3:c.1780+40dup NP_000825.2:n.1780+40dup
XM_011520628.1:c.1780+40dup XP_011518930.1:n.1780+40dup
XM_011520629.1:c.1780+40dup XP_011518931.1:n.1780+40dup
XM_011520630.1:c.1780+40dup XP_011518932.1:n.1780+40dup
XR_931372.1:n.179-3407dup
XR_931373.1:n.318+2934dup
XR_931374.1:n.117+1091dup
NM_000834.4:c.1780+40dup NP_000825.2:n.1780+40dup
XM_011520628.2:c.1780+40dup XP_011518930.1:n.1780+40dup
XM_011520629.2:c.1780+40dup XP_011518931.1:n.1780+40dup
XM_017019219.2:c.1780+40dup XP_016874708.1:n.1780+40dup
XR_001749013.1:n.599+1091dup
XR_931372.2:n.316-3407dup
XR_931373.2:n.457+2934dup
NM_000834.5:c.1780+40dup MANE Select NP_000825.2:n.1780+40dup