Canonical Allele Identifier: CA2017614118

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1867335784

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13944902T>C , CM000674.2:g.13944902T>C	GRCh38
NC_000012.11:g.14097836T>C , CM000674.1:g.14097836T>C	GRCh37
NC_000012.10:g.13989103T>C	NCBI36
NG_031854.1:g.40187A>G
NG_031854.2:g.42111A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.-19+35026A>G MANE Select	ENSP00000477455.1:n.-19+35026A>G
ENST00000630791.2:c.-19+35026A>G	ENSP00000486677.2:n.-19+35026A>G
ENST00000609686.3:c.-19+35026A>G	ENSP00000477455.1:n.-19+35026A>G
ENST00000627535.2:c.-19+35026A>G	ENSP00000486411.1:n.-19+35026A>G
ENST00000630791.1:c.-19+35026A>G	ENSP00000486677.1:n.-19+35026A>G
NM_000834.3:c.-19+35026A>G	NP_000825.2:n.-19+35026A>G
XM_011520628.1:c.-19+35026A>G	XP_011518930.1:n.-19+35026A>G
XM_011520629.1:c.-19+35026A>G	XP_011518931.1:n.-19+35026A>G
XM_011520630.1:c.-19+35026A>G	XP_011518932.1:n.-19+35026A>G
NM_000834.4:c.-19+35026A>G	NP_000825.2:n.-19+35026A>G
XM_011520628.2:c.-19+35026A>G	XP_011518930.1:n.-19+35026A>G
XM_011520629.2:c.-19+35026A>G	XP_011518931.1:n.-19+35026A>G
XM_017019219.2:c.-19+35026A>G	XP_016874708.1:n.-19+35026A>G
NM_000834.5:c.-19+35026A>G MANE Select	NP_000825.2:n.-19+35026A>G