Canonical Allele Identifier: CA384053985
Gene: GRIN2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13753674T>G , CM000674.2:g.13753674T>G GRCh38
NC_000012.11:g.13906608T>G , CM000674.1:g.13906608T>G GRCh37
NC_000012.10:g.13797875T>G NCBI36
NG_031854.1:g.231415A>C
NG_031854.2:g.233339A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.653A>C MANE Select ENSP00000477455.1:p.Asn218Thr
ENST00000630791.2:c.653A>C ENSP00000486677.2:p.Asn218Thr
ENST00000609686.3:c.653A>C ENSP00000477455.1:p.Asn218Thr
NM_000834.3:c.653A>C NP_000825.2:p.Asn218Thr
XM_011520628.1:c.653A>C XP_011518930.1:p.Asn218Thr
XM_011520629.1:c.653A>C XP_011518931.1:p.Asn218Thr
XM_011520630.1:c.653A>C XP_011518932.1:p.Asn218Thr
NM_000834.4:c.653A>C NP_000825.2:p.Asn218Thr
XM_011520628.2:c.653A>C XP_011518930.1:p.Asn218Thr
XM_011520629.2:c.653A>C XP_011518931.1:p.Asn218Thr
XM_017019219.2:c.653A>C XP_016874708.1:p.Asn218Thr
NM_000834.5:c.653A>C MANE Select NP_000825.2:p.Asn218Thr