Canonical Allele Identifier: CA2017578143

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1865816797
• gnomAD v4: 12-13865773-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13865773C>T , CM000674.2:g.13865773C>T	GRCh38
NC_000012.11:g.14018707C>T , CM000674.1:g.14018707C>T	GRCh37
NC_000012.10:g.13909974C>T	NCBI36
NG_031854.1:g.119316G>A
NG_031854.2:g.121240G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.411+25G>A MANE Select	ENSP00000477455.1:n.411+25G>A
ENST00000630791.2:c.411+25G>A	ENSP00000486677.2:n.411+25G>A
ENST00000609686.3:c.411+25G>A	ENSP00000477455.1:n.411+25G>A
NM_000834.3:c.411+25G>A	NP_000825.2:n.411+25G>A
XM_011520628.1:c.411+25G>A	XP_011518930.1:n.411+25G>A
XM_011520629.1:c.411+25G>A	XP_011518931.1:n.411+25G>A
XM_011520630.1:c.411+25G>A	XP_011518932.1:n.411+25G>A
NM_000834.4:c.411+25G>A	NP_000825.2:n.411+25G>A
XM_011520628.2:c.411+25G>A	XP_011518930.1:n.411+25G>A
XM_011520629.2:c.411+25G>A	XP_011518931.1:n.411+25G>A
XM_017019219.2:c.411+25G>A	XP_016874708.1:n.411+25G>A
NM_000834.5:c.411+25G>A MANE Select	NP_000825.2:n.411+25G>A