Canonical Allele Identifier: CA2017465299

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1565478617

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13617307A>G , CM000674.2:g.13617307A>G	GRCh38
NC_000012.11:g.13770241A>G , CM000674.1:g.13770241A>G	GRCh37
NC_000012.10:g.13661508A>G	NCBI36
NG_031854.1:g.367782T>C
NG_031854.2:g.369706T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.1126-650T>C MANE Select	ENSP00000477455.1:n.1126-650T>C
ENST00000630791.2:c.1126-650T>C	ENSP00000486677.2:n.1126-650T>C
ENST00000609686.3:c.1126-650T>C	ENSP00000477455.1:n.1126-650T>C
NM_000834.3:c.1126-650T>C	NP_000825.2:n.1126-650T>C
XM_011520628.1:c.1126-650T>C	XP_011518930.1:n.1126-650T>C
XM_011520629.1:c.1126-650T>C	XP_011518931.1:n.1126-650T>C
XM_011520630.1:c.1126-650T>C	XP_011518932.1:n.1126-650T>C
XR_931372.1:n.307+2081A>G
XR_931373.1:n.447+2081A>G
XR_931374.1:n.246+2081A>G
NM_000834.4:c.1126-650T>C	NP_000825.2:n.1126-650T>C
XM_011520628.2:c.1126-650T>C	XP_011518930.1:n.1126-650T>C
XM_011520629.2:c.1126-650T>C	XP_011518931.1:n.1126-650T>C
XM_017019219.2:c.1126-650T>C	XP_016874708.1:n.1126-650T>C
XR_001749013.1:n.728+2081A>G
XR_931372.2:n.444+2081A>G
XR_931373.2:n.586+2081A>G
NM_000834.5:c.1126-650T>C MANE Select	NP_000825.2:n.1126-650T>C