Canonical Allele Identifier: CA2617757694

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13866373-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13866374_13866375del , CM000674.2:g.13866374_13866375del	GRCh38
NC_000012.11:g.14019308_14019309del , CM000674.1:g.14019308_14019309del	GRCh37
NC_000012.10:g.13910575_13910576del	NCBI36
NG_031854.1:g.118714_118715del
NG_031854.2:g.120638_120639del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.-18-149_-18-148del MANE Select	ENSP00000477455.1:n.-18-149_-18-148del
ENST00000630791.2:c.-18-149_-18-148del	ENSP00000486677.2:n.-18-149_-18-148del
ENST00000609686.3:c.-18-149_-18-148del	ENSP00000477455.1:n.-18-149_-18-148del
ENST00000627535.2:c.-18-149_-18-148del	ENSP00000486411.1:n.-18-149_-18-148del
ENST00000630791.1:c.-18-149_-18-148del	ENSP00000486677.1:n.-18-149_-18-148del
NM_000834.3:c.-18-149_-18-148del	NP_000825.2:n.-18-149_-18-148del
XM_011520628.1:c.-18-149_-18-148del	XP_011518930.1:n.-18-149_-18-148del
XM_011520629.1:c.-18-149_-18-148del	XP_011518931.1:n.-18-149_-18-148del
XM_011520630.1:c.-18-149_-18-148del	XP_011518932.1:n.-18-149_-18-148del
NM_000834.4:c.-18-149_-18-148del	NP_000825.2:n.-18-149_-18-148del
XM_011520628.2:c.-18-149_-18-148del	XP_011518930.1:n.-18-149_-18-148del
XM_011520629.2:c.-18-149_-18-148del	XP_011518931.1:n.-18-149_-18-148del
XM_017019219.2:c.-18-149_-18-148del	XP_016874708.1:n.-18-149_-18-148del
NM_000834.5:c.-18-149_-18-148del MANE Select	NP_000825.2:n.-18-149_-18-148del