Canonical Allele Identifier: CA2017463241

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1949424922

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615450_13615454del , CM000674.2:g.13615450_13615454del	GRCh38
NC_000012.11:g.13768384_13768388del , CM000674.1:g.13768384_13768388del	GRCh37
NC_000012.10:g.13659651_13659655del	NCBI36
NG_031854.1:g.369638_369642del
NG_031854.2:g.371562_371566del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1500+42_1500+46del MANE Select	ENSP00000477455.1:n.1500+42_1500+46del
ENST00000609686.3:c.1500+42_1500+46del	ENSP00000477455.1:n.1500+42_1500+46del
NM_000834.3:c.1500+42_1500+46del	NP_000825.2:n.1500+42_1500+46del
XM_011520628.1:c.1500+42_1500+46del	XP_011518930.1:n.1500+42_1500+46del
XM_011520629.1:c.1500+42_1500+46del	XP_011518931.1:n.1500+42_1500+46del
XM_011520630.1:c.1500+42_1500+46del	XP_011518932.1:n.1500+42_1500+46del
XR_931372.1:n.307+224_307+228del
XR_931373.1:n.447+224_447+228del
XR_931374.1:n.246+224_246+228del
NM_000834.4:c.1500+42_1500+46del	NP_000825.2:n.1500+42_1500+46del
XM_011520628.2:c.1500+42_1500+46del	XP_011518930.1:n.1500+42_1500+46del
XM_011520629.2:c.1500+42_1500+46del	XP_011518931.1:n.1500+42_1500+46del
XM_017019219.2:c.1500+42_1500+46del	XP_016874708.1:n.1500+42_1500+46del
XR_001749013.1:n.728+224_728+228del
XR_931372.2:n.444+224_444+228del
XR_931373.2:n.586+224_586+228del
NM_000834.5:c.1500+42_1500+46del MANE Select	NP_000825.2:n.1500+42_1500+46del