Canonical Allele Identifier: CA2617757605

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13866252-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13866256dup , CM000674.2:g.13866256dup	GRCh38
NC_000012.11:g.14019190dup , CM000674.1:g.14019190dup	GRCh37
NC_000012.10:g.13910457dup	NCBI36
NG_031854.1:g.118836dup
NG_031854.2:g.120760dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.-18-27dup MANE Select	ENSP00000477455.1:n.-18-27dup
ENST00000630791.2:c.-18-27dup	ENSP00000486677.2:n.-18-27dup
ENST00000609686.3:c.-18-27dup	ENSP00000477455.1:n.-18-27dup
ENST00000627535.2:c.-18-27dup	ENSP00000486411.1:n.-18-27dup
ENST00000630791.1:c.-18-27dup	ENSP00000486677.1:n.-18-27dup
NM_000834.3:c.-18-27dup	NP_000825.2:n.-18-27dup
XM_011520628.1:c.-18-27dup	XP_011518930.1:n.-18-27dup
XM_011520629.1:c.-18-27dup	XP_011518931.1:n.-18-27dup
XM_011520630.1:c.-18-27dup	XP_011518932.1:n.-18-27dup
NM_000834.4:c.-18-27dup	NP_000825.2:n.-18-27dup
XM_011520628.2:c.-18-27dup	XP_011518930.1:n.-18-27dup
XM_011520629.2:c.-18-27dup	XP_011518931.1:n.-18-27dup
XM_017019219.2:c.-18-27dup	XP_016874708.1:n.-18-27dup
NM_000834.5:c.-18-27dup MANE Select	NP_000825.2:n.-18-27dup