Canonical Allele Identifier: CA233159110
Gene: GRIN2B HGNC NCBI

Linked Data

dbSNP Id: rs182446504

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13962553C>T , CM000674.2:g.13962553C>T GRCh38
NC_000012.11:g.14115487C>T , CM000674.1:g.14115487C>T GRCh37
NC_000012.10:g.14006754C>T NCBI36
NG_031854.1:g.22536G>A
NG_031854.2:g.24460G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.-19+17375G>A MANE Select ENSP00000477455.1:n.-19+17375G>A
ENST00000630791.2:c.-19+17375G>A ENSP00000486677.2:n.-19+17375G>A
ENST00000609686.3:c.-19+17375G>A ENSP00000477455.1:n.-19+17375G>A
ENST00000627535.2:c.-19+17375G>A ENSP00000486411.1:n.-19+17375G>A
ENST00000630791.1:c.-19+17375G>A ENSP00000486677.1:n.-19+17375G>A
NM_000834.3:c.-19+17375G>A NP_000825.2:n.-19+17375G>A
XM_011520628.1:c.-19+17375G>A XP_011518930.1:n.-19+17375G>A
XM_011520629.1:c.-19+17375G>A XP_011518931.1:n.-19+17375G>A
XM_011520630.1:c.-19+17375G>A XP_011518932.1:n.-19+17375G>A
NM_000834.4:c.-19+17375G>A NP_000825.2:n.-19+17375G>A
XM_011520628.2:c.-19+17375G>A XP_011518930.1:n.-19+17375G>A
XM_011520629.2:c.-19+17375G>A XP_011518931.1:n.-19+17375G>A
XM_017019219.2:c.-19+17375G>A XP_016874708.1:n.-19+17375G>A
NM_000834.5:c.-19+17375G>A MANE Select NP_000825.2:n.-19+17375G>A