Canonical Allele Identifier: CA2617717727
Gene: GRIN2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13561281C>A , CM000674.2:g.13561281C>A GRCh38
NC_000012.11:g.13714215C>A , CM000674.1:g.13714215C>A GRCh37
NC_000012.10:g.13605482C>A NCBI36
NG_031854.1:g.423808G>T
NG_031854.2:g.425732G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.*1502G>T MANE Select ENSP00000477455.1:n.*1502G>T
ENST00000637214.1:c.69+47322G>T ENSP00000489997.1:n.69+47322G>T
ENST00000609686.3:c.*1502G>T ENSP00000477455.1:n.*1502G>T
XM_005253351.2:c.*1502G>T XP_005253408.1:n.*1502G>T
XM_011520628.1:c.*1502G>T XP_011518930.1:n.*1502G>T
XM_011520629.1:c.*1502G>T XP_011518931.1:n.*1502G>T
XM_011520630.1:c.*1502G>T XP_011518932.1:n.*1502G>T
NM_000834.4:c.*1502G>T NP_000825.2:n.*1502G>T
XM_005253351.3:c.*1502G>T XP_005253408.1:n.*1502G>T
XM_011520628.2:c.*1502G>T XP_011518930.1:n.*1502G>T
XM_011520629.2:c.*1502G>T XP_011518931.1:n.*1502G>T
XM_017019219.2:c.*1502G>T XP_016874708.1:n.*1502G>T
NM_000834.5:c.*1502G>T MANE Select NP_000825.2:n.*1502G>T