Canonical Allele Identifier: CA2017465294

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1949457362

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13617303G>A , CM000674.2:g.13617303G>A	GRCh38
NC_000012.11:g.13770237G>A , CM000674.1:g.13770237G>A	GRCh37
NC_000012.10:g.13661504G>A	NCBI36
NG_031854.1:g.367786C>T
NG_031854.2:g.369710C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.1126-646C>T MANE Select	ENSP00000477455.1:n.1126-646C>T
ENST00000630791.2:c.1126-646C>T	ENSP00000486677.2:n.1126-646C>T
ENST00000609686.3:c.1126-646C>T	ENSP00000477455.1:n.1126-646C>T
NM_000834.3:c.1126-646C>T	NP_000825.2:n.1126-646C>T
XM_011520628.1:c.1126-646C>T	XP_011518930.1:n.1126-646C>T
XM_011520629.1:c.1126-646C>T	XP_011518931.1:n.1126-646C>T
XM_011520630.1:c.1126-646C>T	XP_011518932.1:n.1126-646C>T
XR_931372.1:n.307+2077G>A
XR_931373.1:n.447+2077G>A
XR_931374.1:n.246+2077G>A
NM_000834.4:c.1126-646C>T	NP_000825.2:n.1126-646C>T
XM_011520628.2:c.1126-646C>T	XP_011518930.1:n.1126-646C>T
XM_011520629.2:c.1126-646C>T	XP_011518931.1:n.1126-646C>T
XM_017019219.2:c.1126-646C>T	XP_016874708.1:n.1126-646C>T
XR_001749013.1:n.728+2077G>A
XR_931372.2:n.444+2077G>A
XR_931373.2:n.586+2077G>A
NM_000834.5:c.1126-646C>T MANE Select	NP_000825.2:n.1126-646C>T