Canonical Allele Identifier: CA2617718489

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13562589-AAAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562590_13562592del , CM000674.2:g.13562590_13562592del	GRCh38
NC_000012.11:g.13715524_13715526del , CM000674.1:g.13715524_13715526del	GRCh37
NC_000012.10:g.13606791_13606793del	NCBI36
NG_031854.1:g.422497_422499del
NG_031854.2:g.424421_424423del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*191_*193del MANE Select	ENSP00000477455.1:n.*191_*193del
ENST00000637214.1:c.69+46011_69+46013del	ENSP00000489997.1:n.69+46011_69+46013del
ENST00000609686.3:c.*191_*193del	ENSP00000477455.1:n.*191_*193del
NM_000834.3:c.*191_*193del	NP_000825.2:n.*191_*193del
XM_005253351.2:c.*191_*193del	XP_005253408.1:n.*191_*193del
XM_011520628.1:c.*191_*193del	XP_011518930.1:n.*191_*193del
XM_011520629.1:c.*191_*193del	XP_011518931.1:n.*191_*193del
XM_011520630.1:c.*191_*193del	XP_011518932.1:n.*191_*193del
NM_000834.4:c.*191_*193del	NP_000825.2:n.*191_*193del
XM_005253351.3:c.*191_*193del	XP_005253408.1:n.*191_*193del
XM_011520628.2:c.*191_*193del	XP_011518930.1:n.*191_*193del
XM_011520629.2:c.*191_*193del	XP_011518931.1:n.*191_*193del
XM_017019219.2:c.*191_*193del	XP_016874708.1:n.*191_*193del
NM_000834.5:c.*191_*193del MANE Select	NP_000825.2:n.*191_*193del