Canonical Allele Identifier: CA233131971
Gene: GRIN2B HGNC NCBI

Linked Data

dbSNP Id: rs959405813

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13562321T>C , CM000674.2:g.13562321T>C GRCh38
NC_000012.11:g.13715255T>C , CM000674.1:g.13715255T>C GRCh37
NC_000012.10:g.13606522T>C NCBI36
NG_031854.1:g.422768A>G
NG_031854.2:g.424692A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.*462A>G MANE Select ENSP00000477455.1:n.*462A>G
ENST00000637214.1:c.69+46282A>G ENSP00000489997.1:n.69+46282A>G
ENST00000609686.3:c.*462A>G ENSP00000477455.1:n.*462A>G
NM_000834.3:c.*462A>G NP_000825.2:n.*462A>G
XM_005253351.2:c.*462A>G XP_005253408.1:n.*462A>G
XM_011520628.1:c.*462A>G XP_011518930.1:n.*462A>G
XM_011520629.1:c.*462A>G XP_011518931.1:n.*462A>G
XM_011520630.1:c.*462A>G XP_011518932.1:n.*462A>G
NM_000834.4:c.*462A>G NP_000825.2:n.*462A>G
XM_005253351.3:c.*462A>G XP_005253408.1:n.*462A>G
XM_011520628.2:c.*462A>G XP_011518930.1:n.*462A>G
XM_011520629.2:c.*462A>G XP_011518931.1:n.*462A>G
XM_017019219.2:c.*462A>G XP_016874708.1:n.*462A>G
NM_000834.5:c.*462A>G MANE Select NP_000825.2:n.*462A>G