Canonical Allele Identifier: CA2017438767

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1948642712

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13566479_13566482dup , CM000674.2:g.13566479_13566482dup	GRCh38
NC_000012.11:g.13719413_13719416dup , CM000674.1:g.13719413_13719416dup	GRCh37
NC_000012.10:g.13610680_13610683dup	NCBI36
NG_031854.1:g.418609_418612dup
NG_031854.2:g.420533_420536dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.2598+545_2598+548dup MANE Select	ENSP00000477455.1:n.2598+545_2598+548dup
ENST00000637214.1:c.69+42123_69+42126dup	ENSP00000489997.1:n.69+42123_69+42126dup
ENST00000609686.3:c.2598+545_2598+548dup	ENSP00000477455.1:n.2598+545_2598+548dup
ENST00000628166.1:n.858+545_858+548dup
NM_000834.3:c.2598+545_2598+548dup	NP_000825.2:n.2598+545_2598+548dup
XM_005253351.2:c.384+545_384+548dup	XP_005253408.1:n.384+545_384+548dup
XM_011520628.1:c.2598+545_2598+548dup	XP_011518930.1:n.2598+545_2598+548dup
XM_011520629.1:c.2598+545_2598+548dup	XP_011518931.1:n.2598+545_2598+548dup
XM_011520630.1:c.2598+545_2598+548dup	XP_011518932.1:n.2598+545_2598+548dup
NM_000834.4:c.2598+545_2598+548dup	NP_000825.2:n.2598+545_2598+548dup
XM_005253351.3:c.384+545_384+548dup	XP_005253408.1:n.384+545_384+548dup
XM_011520628.2:c.2598+545_2598+548dup	XP_011518930.1:n.2598+545_2598+548dup
XM_011520629.2:c.2598+545_2598+548dup	XP_011518931.1:n.2598+545_2598+548dup
XM_017019219.2:c.2598+545_2598+548dup	XP_016874708.1:n.2598+545_2598+548dup
NM_000834.5:c.2598+545_2598+548dup MANE Select	NP_000825.2:n.2598+545_2598+548dup