Canonical Allele Identifier: CA603465605
Gene: GRIN2B HGNC NCBI

Linked Data

dbSNP Id: rs1162293700

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13962530A>G , CM000674.2:g.13962530A>G GRCh38
NC_000012.11:g.14115464A>G , CM000674.1:g.14115464A>G GRCh37
NC_000012.10:g.14006731A>G NCBI36
NG_031854.1:g.22559T>C
NG_031854.2:g.24483T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.-19+17398T>C MANE Select ENSP00000477455.1:n.-19+17398T>C
ENST00000630791.2:c.-19+17398T>C ENSP00000486677.2:n.-19+17398T>C
ENST00000609686.3:c.-19+17398T>C ENSP00000477455.1:n.-19+17398T>C
ENST00000627535.2:c.-19+17398T>C ENSP00000486411.1:n.-19+17398T>C
ENST00000630791.1:c.-19+17398T>C ENSP00000486677.1:n.-19+17398T>C
NM_000834.3:c.-19+17398T>C NP_000825.2:n.-19+17398T>C
XM_011520628.1:c.-19+17398T>C XP_011518930.1:n.-19+17398T>C
XM_011520629.1:c.-19+17398T>C XP_011518931.1:n.-19+17398T>C
XM_011520630.1:c.-19+17398T>C XP_011518932.1:n.-19+17398T>C
NM_000834.4:c.-19+17398T>C NP_000825.2:n.-19+17398T>C
XM_011520628.2:c.-19+17398T>C XP_011518930.1:n.-19+17398T>C
XM_011520629.2:c.-19+17398T>C XP_011518931.1:n.-19+17398T>C
XM_017019219.2:c.-19+17398T>C XP_016874708.1:n.-19+17398T>C
NM_000834.5:c.-19+17398T>C MANE Select NP_000825.2:n.-19+17398T>C