Canonical Allele Identifier: CA384053489
Gene: GRIN2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13753546G>C , CM000674.2:g.13753546G>C GRCh38
NC_000012.11:g.13906480G>C , CM000674.1:g.13906480G>C GRCh37
NC_000012.10:g.13797747G>C NCBI36
NG_031854.1:g.231543C>G
NG_031854.2:g.233467C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.781C>G MANE Select ENSP00000477455.1:p.Leu261Val
ENST00000630791.2:c.781C>G ENSP00000486677.2:p.Leu261Val
ENST00000609686.3:c.781C>G ENSP00000477455.1:p.Leu261Val
NM_000834.3:c.781C>G NP_000825.2:p.Leu261Val
XM_011520628.1:c.781C>G XP_011518930.1:p.Leu261Val
XM_011520629.1:c.781C>G XP_011518931.1:p.Leu261Val
XM_011520630.1:c.781C>G XP_011518932.1:p.Leu261Val
NM_000834.4:c.781C>G NP_000825.2:p.Leu261Val
XM_011520628.2:c.781C>G XP_011518930.1:p.Leu261Val
XM_011520629.2:c.781C>G XP_011518931.1:p.Leu261Val
XM_017019219.2:c.781C>G XP_016874708.1:p.Leu261Val
NM_000834.5:c.781C>G MANE Select NP_000825.2:p.Leu261Val