Canonical Allele Identifier: CA685683605
Gene: GRIN2B HGNC NCBI

Linked Data

dbSNP Id: rs1284739660

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13719066A>C , CM000674.2:g.13719066A>C GRCh38
NC_000012.11:g.13872000A>C , CM000674.1:g.13872000A>C GRCh37
NC_000012.10:g.13763267A>C NCBI36
NG_031854.1:g.266023T>G
NG_031854.2:g.267947T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.1010+34251T>G MANE Select ENSP00000477455.1:n.1010+34251T>G
ENST00000630791.2:c.1010+34251T>G ENSP00000486677.2:n.1010+34251T>G
ENST00000609686.3:c.1010+34251T>G ENSP00000477455.1:n.1010+34251T>G
NM_000834.3:c.1010+34251T>G NP_000825.2:n.1010+34251T>G
XM_011520628.1:c.1010+34251T>G XP_011518930.1:n.1010+34251T>G
XM_011520629.1:c.1010+34251T>G XP_011518931.1:n.1010+34251T>G
XM_011520630.1:c.1010+34251T>G XP_011518932.1:n.1010+34251T>G
NM_000834.4:c.1010+34251T>G NP_000825.2:n.1010+34251T>G
XM_011520628.2:c.1010+34251T>G XP_011518930.1:n.1010+34251T>G
XM_011520629.2:c.1010+34251T>G XP_011518931.1:n.1010+34251T>G
XM_017019219.2:c.1010+34251T>G XP_016874708.1:n.1010+34251T>G
NM_000834.5:c.1010+34251T>G MANE Select NP_000825.2:n.1010+34251T>G