Canonical Allele Identifier: CA233130998
Gene: GRIN2B HGNC NCBI

Linked Data

dbSNP Id: rs186973533

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13561050G>C , CM000674.2:g.13561050G>C GRCh38
NC_000012.11:g.13713984G>C , CM000674.1:g.13713984G>C GRCh37
NC_000012.10:g.13605251G>C NCBI36
NG_031854.1:g.424039C>G
NG_031854.2:g.425963C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.*1733C>G MANE Select ENSP00000477455.1:n.*1733C>G
ENST00000637214.1:c.69+47553C>G ENSP00000489997.1:n.69+47553C>G
ENST00000609686.3:c.*1733C>G ENSP00000477455.1:n.*1733C>G
XM_005253351.2:c.*1733C>G XP_005253408.1:n.*1733C>G
XM_011520628.1:c.*1733C>G XP_011518930.1:n.*1733C>G
XM_011520629.1:c.*1733C>G XP_011518931.1:n.*1733C>G
XM_011520630.1:c.*1733C>G XP_011518932.1:n.*1733C>G
NM_000834.4:c.*1733C>G NP_000825.2:n.*1733C>G
XM_005253351.3:c.*1733C>G XP_005253408.1:n.*1733C>G
XM_011520628.2:c.*1733C>G XP_011518930.1:n.*1733C>G
XM_011520629.2:c.*1733C>G XP_011518931.1:n.*1733C>G
XM_017019219.2:c.*1733C>G XP_016874708.1:n.*1733C>G
NM_000834.5:c.*1733C>G MANE Select NP_000825.2:n.*1733C>G