Canonical Allele Identifier: CA2581062769

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13866223C>G , CM000674.2:g.13866223C>G	GRCh38
NC_000012.11:g.14019157C>G , CM000674.1:g.14019157C>G	GRCh37
NC_000012.10:g.13910424C>G	NCBI36
NG_031854.1:g.118866G>C
NG_031854.2:g.120790G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.-15G>C MANE Select	ENSP00000477455.1:n.-15G>C
ENST00000630791.2:c.-15G>C	ENSP00000486677.2:n.-15G>C
ENST00000609686.3:c.-15G>C	ENSP00000477455.1:n.-15G>C
ENST00000627535.2:c.-15G>C	ENSP00000486411.1:n.-15G>C
ENST00000630791.1:c.-15G>C	ENSP00000486677.1:n.-15G>C
NM_000834.3:c.-15G>C	NP_000825.2:n.-15G>C
XM_011520628.1:c.-15G>C	XP_011518930.1:n.-15G>C
XM_011520629.1:c.-15G>C	XP_011518931.1:n.-15G>C
XM_011520630.1:c.-15G>C	XP_011518932.1:n.-15G>C
NM_000834.4:c.-15G>C	NP_000825.2:n.-15G>C
XM_011520628.2:c.-15G>C	XP_011518930.1:n.-15G>C
XM_011520629.2:c.-15G>C	XP_011518931.1:n.-15G>C
XM_017019219.2:c.-15G>C	XP_016874708.1:n.-15G>C
NM_000834.5:c.-15G>C MANE Select	NP_000825.2:n.-15G>C