Canonical Allele Identifier: CA2617751747

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13615684-A-AAAAC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615696_13615699dup , CM000674.2:g.13615696_13615699dup	GRCh38
NC_000012.11:g.13768630_13768633dup , CM000674.1:g.13768630_13768633dup	GRCh37
NC_000012.10:g.13659897_13659900dup	NCBI36
NG_031854.1:g.369401_369404dup
NG_031854.2:g.371325_371328dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1329-24_1329-21dup MANE Select	ENSP00000477455.1:n.1329-24_1329-21dup
ENST00000630791.2:c.1329-24_1329-21dup	ENSP00000486677.2:n.1329-24_1329-21dup
ENST00000609686.3:c.1329-24_1329-21dup	ENSP00000477455.1:n.1329-24_1329-21dup
NM_000834.3:c.1329-24_1329-21dup	NP_000825.2:n.1329-24_1329-21dup
XM_011520628.1:c.1329-24_1329-21dup	XP_011518930.1:n.1329-24_1329-21dup
XM_011520629.1:c.1329-24_1329-21dup	XP_011518931.1:n.1329-24_1329-21dup
XM_011520630.1:c.1329-24_1329-21dup	XP_011518932.1:n.1329-24_1329-21dup
XR_931372.1:n.307+470_307+473dup
XR_931373.1:n.447+470_447+473dup
XR_931374.1:n.246+470_246+473dup
NM_000834.4:c.1329-24_1329-21dup	NP_000825.2:n.1329-24_1329-21dup
XM_011520628.2:c.1329-24_1329-21dup	XP_011518930.1:n.1329-24_1329-21dup
XM_011520629.2:c.1329-24_1329-21dup	XP_011518931.1:n.1329-24_1329-21dup
XM_017019219.2:c.1329-24_1329-21dup	XP_016874708.1:n.1329-24_1329-21dup
XR_001749013.1:n.728+470_728+473dup
XR_931372.2:n.444+470_444+473dup
XR_931373.2:n.586+470_586+473dup
NM_000834.5:c.1329-24_1329-21dup MANE Select	NP_000825.2:n.1329-24_1329-21dup