Canonical Allele Identifier: CA384055183

Gene: GRIN2B

Linked Data

• dbSNP Id: rs749839263
• MyVariant Identifiers: chr12:g.14019133T>A (hg19) ; chr12:g.13866199T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13866199T>A , CM000674.2:g.13866199T>A	GRCh38
NC_000012.11:g.14019133T>A , CM000674.1:g.14019133T>A	GRCh37
NC_000012.10:g.13910400T>A	NCBI36
NG_031854.1:g.118890A>T
NG_031854.2:g.120814A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.10A>T MANE Select	ENSP00000477455.1:p.Arg4Ter
ENST00000630791.2:c.10A>T	ENSP00000486677.2:p.Arg4Ter
ENST00000609686.3:c.10A>T	ENSP00000477455.1:p.Arg4Ter
ENST00000627535.2:c.10A>T	ENSP00000486411.1:p.Arg4Ter
ENST00000630791.1:c.10A>T	ENSP00000486677.1:p.Arg4Ter
NM_000834.3:c.10A>T	NP_000825.2:p.Arg4Ter
XM_011520628.1:c.10A>T	XP_011518930.1:p.Arg4Ter
XM_011520629.1:c.10A>T	XP_011518931.1:p.Arg4Ter
XM_011520630.1:c.10A>T	XP_011518932.1:p.Arg4Ter
NM_000834.4:c.10A>T	NP_000825.2:p.Arg4Ter
XM_011520628.2:c.10A>T	XP_011518930.1:p.Arg4Ter
XM_011520629.2:c.10A>T	XP_011518931.1:p.Arg4Ter
XM_017019219.2:c.10A>T	XP_016874708.1:p.Arg4Ter
NM_000834.5:c.10A>T MANE Select	NP_000825.2:p.Arg4Ter