Canonical Allele Identifier: CA944948029

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1865817193
• gnomAD v3: 12-13865795-T-A
• gnomAD v4: 12-13865795-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13865795T>A , CM000674.2:g.13865795T>A	GRCh38
NC_000012.11:g.14018729T>A , CM000674.1:g.14018729T>A	GRCh37
NC_000012.10:g.13909996T>A	NCBI36
NG_031854.1:g.119294A>T
NG_031854.2:g.121218A>T

Transcript Alleles

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