Canonical Allele Identifier: CA2725498839
Gene: GRIN2B HGNC NCBI

Linked Data

dbSNP Id: rs2136399927
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13561336C>T , CM000674.2:g.13561336C>T GRCh38
NC_000012.11:g.13714270C>T , CM000674.1:g.13714270C>T GRCh37
NC_000012.10:g.13605537C>T NCBI36
NG_031854.1:g.423753G>A
NG_031854.2:g.425677G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.*1447G>A MANE Select ENSP00000477455.1:n.*1447G>A
ENST00000637214.1:c.69+47267G>A ENSP00000489997.1:n.69+47267G>A
ENST00000609686.3:c.*1447G>A ENSP00000477455.1:n.*1447G>A
XM_005253351.2:c.*1447G>A XP_005253408.1:n.*1447G>A
XM_011520628.1:c.*1447G>A XP_011518930.1:n.*1447G>A
XM_011520629.1:c.*1447G>A XP_011518931.1:n.*1447G>A
XM_011520630.1:c.*1447G>A XP_011518932.1:n.*1447G>A
NM_000834.4:c.*1447G>A NP_000825.2:n.*1447G>A
XM_005253351.3:c.*1447G>A XP_005253408.1:n.*1447G>A
XM_011520628.2:c.*1447G>A XP_011518930.1:n.*1447G>A
XM_011520629.2:c.*1447G>A XP_011518931.1:n.*1447G>A
XM_017019219.2:c.*1447G>A XP_016874708.1:n.*1447G>A
NM_000834.5:c.*1447G>A MANE Select NP_000825.2:n.*1447G>A
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