Canonical Allele Identifier: CA685693175
Gene: GRIN2B HGNC NCBI

Linked Data

dbSNP Id: rs1240356049

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13962630G>A , CM000674.2:g.13962630G>A GRCh38
NC_000012.11:g.14115564G>A , CM000674.1:g.14115564G>A GRCh37
NC_000012.10:g.14006831G>A NCBI36
NG_031854.1:g.22459C>T
NG_031854.2:g.24383C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.-19+17298C>T MANE Select ENSP00000477455.1:n.-19+17298C>T
ENST00000630791.2:c.-19+17298C>T ENSP00000486677.2:n.-19+17298C>T
ENST00000609686.3:c.-19+17298C>T ENSP00000477455.1:n.-19+17298C>T
ENST00000627535.2:c.-19+17298C>T ENSP00000486411.1:n.-19+17298C>T
ENST00000630791.1:c.-19+17298C>T ENSP00000486677.1:n.-19+17298C>T
NM_000834.3:c.-19+17298C>T NP_000825.2:n.-19+17298C>T
XM_011520628.1:c.-19+17298C>T XP_011518930.1:n.-19+17298C>T
XM_011520629.1:c.-19+17298C>T XP_011518931.1:n.-19+17298C>T
XM_011520630.1:c.-19+17298C>T XP_011518932.1:n.-19+17298C>T
NM_000834.4:c.-19+17298C>T NP_000825.2:n.-19+17298C>T
XM_011520628.2:c.-19+17298C>T XP_011518930.1:n.-19+17298C>T
XM_011520629.2:c.-19+17298C>T XP_011518931.1:n.-19+17298C>T
XM_017019219.2:c.-19+17298C>T XP_016874708.1:n.-19+17298C>T
NM_000834.5:c.-19+17298C>T MANE Select NP_000825.2:n.-19+17298C>T