Canonical Allele Identifier: CA233159108
Gene: GRIN2B HGNC NCBI

Linked Data

dbSNP Id: rs373440275

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13962501T>C , CM000674.2:g.13962501T>C GRCh38
NC_000012.11:g.14115435T>C , CM000674.1:g.14115435T>C GRCh37
NC_000012.10:g.14006702T>C NCBI36
NG_031854.1:g.22588A>G
NG_031854.2:g.24512A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.-19+17427A>G MANE Select ENSP00000477455.1:n.-19+17427A>G
ENST00000630791.2:c.-19+17427A>G ENSP00000486677.2:n.-19+17427A>G
ENST00000609686.3:c.-19+17427A>G ENSP00000477455.1:n.-19+17427A>G
ENST00000627535.2:c.-19+17427A>G ENSP00000486411.1:n.-19+17427A>G
ENST00000630791.1:c.-19+17427A>G ENSP00000486677.1:n.-19+17427A>G
NM_000834.3:c.-19+17427A>G NP_000825.2:n.-19+17427A>G
XM_011520628.1:c.-19+17427A>G XP_011518930.1:n.-19+17427A>G
XM_011520629.1:c.-19+17427A>G XP_011518931.1:n.-19+17427A>G
XM_011520630.1:c.-19+17427A>G XP_011518932.1:n.-19+17427A>G
NM_000834.4:c.-19+17427A>G NP_000825.2:n.-19+17427A>G
XM_011520628.2:c.-19+17427A>G XP_011518930.1:n.-19+17427A>G
XM_011520629.2:c.-19+17427A>G XP_011518931.1:n.-19+17427A>G
XM_017019219.2:c.-19+17427A>G XP_016874708.1:n.-19+17427A>G
NM_000834.5:c.-19+17427A>G MANE Select NP_000825.2:n.-19+17427A>G