Canonical Allele Identifier: CA2017465070

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1949453924

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13617072_13617073insTA , CM000674.2:g.13617072_13617073insTA	GRCh38
NC_000012.11:g.13770006_13770007insTA , CM000674.1:g.13770006_13770007insTA	GRCh37
NC_000012.10:g.13661273_13661274insTA	NCBI36
NG_031854.1:g.368016_368017insTA
NG_031854.2:g.369940_369941insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1126-416_1126-415insTA MANE Select	ENSP00000477455.1:n.1126-416_1126-415insTA
ENST00000630791.2:c.1126-416_1126-415insTA	ENSP00000486677.2:n.1126-416_1126-415insTA
ENST00000609686.3:c.1126-416_1126-415insTA	ENSP00000477455.1:n.1126-416_1126-415insTA
NM_000834.3:c.1126-416_1126-415insTA	NP_000825.2:n.1126-416_1126-415insTA
XM_011520628.1:c.1126-416_1126-415insTA	XP_011518930.1:n.1126-416_1126-415insTA
XM_011520629.1:c.1126-416_1126-415insTA	XP_011518931.1:n.1126-416_1126-415insTA
XM_011520630.1:c.1126-416_1126-415insTA	XP_011518932.1:n.1126-416_1126-415insTA
XR_931372.1:n.307+1846_307+1847insTA
XR_931373.1:n.447+1846_447+1847insTA
XR_931374.1:n.246+1846_246+1847insTA
NM_000834.4:c.1126-416_1126-415insTA	NP_000825.2:n.1126-416_1126-415insTA
XM_011520628.2:c.1126-416_1126-415insTA	XP_011518930.1:n.1126-416_1126-415insTA
XM_011520629.2:c.1126-416_1126-415insTA	XP_011518931.1:n.1126-416_1126-415insTA
XM_017019219.2:c.1126-416_1126-415insTA	XP_016874708.1:n.1126-416_1126-415insTA
XR_001749013.1:n.728+1846_728+1847insTA
XR_931372.2:n.444+1846_444+1847insTA
XR_931373.2:n.586+1846_586+1847insTA
NM_000834.5:c.1126-416_1126-415insTA MANE Select	NP_000825.2:n.1126-416_1126-415insTA